xmlns:atom="http://www.w3.org/2005/Atom"
Welsh Statutory Instruments
NATIONAL HEALTH SERVICE, WALES
Made
31 March 2005
Coming into force
1 April 2005
The National Assembly for Wales in exercise of the powers conferred by sections 41, 42, 43 and 126(4) of the National Health Service Act 1977(1) hereby makes the following Regulations:
1.—(1) These Regulations are called the National Health Service (Pharmaceutical Services) (Amendment) (Wales) Regulations 2005 and will come into force on 1 April 2005.
(2) In these Regulations—
“the principal Regulations” means the National Health Service (Pharmaceutical Services) Regulations 1992(2);
(3) These Regulations apply in relation to Wales only.
2.—(1) Regulation 2(1) of the principal Regulations is amended in accordance with the following provisions of this regulation.
(2) For the definition of “supplementary prescriber” substitute—
““supplementary prescriber” means a person—
whose name is registered in—
the Nursing and Midwifery Register,
the Register of Pharmaceutical Chemists maintained in pursuance of section 2(1) of (the registers and registration) of the Pharmacy Act 1954(3), or
the register maintained in pursuance of Articles 6 and 9 of the Pharmacy (Northern Ireland) Order 1976(4), or
the part of the register maintained by the Health Professions Council in pursuance of article 5 of the Health Professions Order 2001(5) relating to —
chiropodists and podiatrists,
physiotherapists,
radiographers: diagnostic or therapeutic; and
against whose name is recorded in the relevant register an annotation signifying that he is qualified to order drugs and appliances as a supplementary prescriber;”.
(3) For the definition of “terms of service” substitute—
““terms of service” means the terms of service contained in or referred to—
in relation to chemists, in Parts 1 to 5 of Schedule 2,
in relation to doctors who provide pharmaceutical services, in Parts 1 and 6 of Schedule 2.”.
(4) In the appropriate places in the alphabetical order, insert the following definitions—
““essential services” has the meaning given in paragraph 3 of Schedule 2;
“NHS services” means services provided as part of the health service continued under section 1(1) of the Act;
“suspended” means—
suspended by a Primary Care Trust or equivalent body under sections 49I (suspension)(6) or 49J(suspension pending appeal) of the Act, regulations made under section 28DA (7)(lists of persons who may perform personal medical services or personal dental services) or 43D (8)supplementary lists) of the Act, or under section 8ZA (list of persons who may perform personal medical services or personal dental services) of the 1997 Act; or
in relation to Scotland or Northern Ireland, suspended under provisions in force corresponding to those in or made under sections 28DA, 43D, 49I or 49J of the Act or under section 8ZA(9) of the 1997 Act,
and shall be treated as including a case where a person is treated as suspended by a Local Health Board, or prior to 1 April 2003, a Health Authority by virtue of regulation 6(2) of the Abolition of the National Health Service Tribunal (Consequential Provisions) Regulations 2002(10), or, in England by a Primary Care Trust or, prior to 1 October 2002, by a Health Authority by virtue of regulation 6(2) of the Abolition of the National Health Service Tribunal (Consequential Provision) Regulations 2001(11), and “suspends” and “suspension” shall be construed accordingly;”.
(5) Omit the following definition—
““repeat dispensing chemist””.
3.—(1) Regulation 4 of the principal Regulations is amended in accordance with the following provisions of this regulation.
(2) In paragraph (1), for “additional professional services under regulation 16A or repeat dispensing services under regulation 16B” substitute “directed services, and if he has, which services.”.
(3) In paragraph (2)(b)(iii) omit the words “other than repeat dispensing services”.
(4) For paragraph (6) substitute the following paragraph—
“(6) A Local Health Board shall refuse an application in which a chemist does not offer to provide all of the essential services, but may grant an application either in respect of all, or in respect of some only, of the directed services specified in it.”.
4. Regulation 16A is omitted.
5. Regulation 16B is omitted.
6. In regulation 18(1), for sub-paragraph (g) substitute the following sub-paragraph—
“(g)the dispensing or other fees or allowances payable in respect of the provision of pharmaceutical services.”.
7. In paragraph 2 of Part I to Schedule 2 to the principal Regulations (incorporation of provisions) after sub-paragraph (c) insert the following sub-paragraph—
“and
(d)so much of regulation 20 of the Community Health Councils Regulations 2004(12) as relate to the entry and inspection of premises either owned or controlled by the chemist or doctor or where pharmaceutical services are provided.”.
8. For Part II of Schedule 2 to the principal Regulations (Terms of Service for Chemists) substitute the following Parts—
3. For the purposes of these Regulations, “essential services” means—
(a)the services described in this Part; and
(b)the activities described in this Part to be carried out in connection with those services.
4. A chemist shall, to the extent that paragraphs 5 to 9 require and in the manner described in those paragraphs, provide proper and sufficient drugs and appliances to persons presenting a prescription for that drug or appliance signed by a health care professional in pursuance of his functions in the health service, the Scottish health service or the Northern Ireland health service.
5.—(1) Subject to the following provisions of this Part, where a person presents on a prescription form—
(a)an order for drugs, not being Scheduled drugs, or for appliances, not being restricted availability appliances, signed by a prescriber;
(b)an order for a drug specified in Schedule 2 to the Prescription of Drugs Regulations, signed by, and endorsed on its face with the reference “SLS” by a prescriber; or
(c)an order for a restricted availability appliance, signed by and endorsed on its face with the reference “SLS” by a prescriber,
a chemist shall, with reasonable promptness and in accordance with any directions given by the prescriber in the prescription form, provide the drugs so ordered, and such of the appliances so ordered as he supplies in the normal course of his business.
(2) Subject to the following provisions of this Part, where any person—
(a)presents a repeatable prescription which contains—
(i)an order for drugs, not being Scheduled drugs or controlled drugs within the meaning of the Misuse of Drugs Act 1971, other than a drug which is for the time being specified in Schedule 4 or 5 to the Misuse of Drugs Regulations 2001, signed by a repeatable prescriber,
(ii)an order for a drug specified in Schedule 2 to the Prescription of Drugs Regulations, not being a controlled drug within the meaning of the Misuse of Drugs Act 1971, other than a drug which is for the time being specified in Schedule 4 or 5 to the Misuse of Drugs Regulations 2001, signed by and endorsed on its face with the reference “SLS” by a repeatable prescriber,
(iii)an order for appliances, not being restricted availability appliances, signed by a repeatable prescriber, or
(iv)an order for a restricted availability appliance, signed by, and endorsed on its face with the reference “SLS” by a repeatable prescriber,
and also presents an associated batch issue; or
(b)requests the provision of drugs or appliances in accordance with a repeatable prescription of a kind specified in paragraph (a),
a chemist shall, with reasonable promptness and in accordance with any directions given by the repeatable prescriber in the repeatable prescription, provide the drugs so ordered, and such of the appliances so ordered as he supplies in the normal course of his business.
(3) For the purposes of this paragraph, a repeatable prescription for drugs or appliances shall be taken to be presented even if the person who wishes to obtain the drugs or appliances does not present that prescription, where—
(a)the chemist has that prescription in his possession; and
(b)that person presents, or the chemist has in his possession, an associated batch issue.
6. Where, in a case of urgency, a prescriber personally known to a chemist requests him to provide a drug, the chemist may provide that drug before receiving a prescription form or repeatable prescription, provided that—
(a)that drug is not a Scheduled drug;
(b)that drug is not a controlled drug within the meaning of the Misuse of Drugs Act 1971, other than a drug which is for the time being specified in Schedules 4 or 5 to the Misuse of Drugs Regulations 2001; and
the prescriber undertakes to give the chemist a prescription form or repeatable prescription in respect of the drug within 72 hours.
7.—(1) If the person presenting the prescription form or repeatable prescription, or requesting the provision of drugs or appliances in accordance with a repeatable prescription, asks the chemist to do so—
(a)the chemist shall give an estimate of the time when the drugs or appliances will be ready; and
(b)if they are not ready by then, the chemist shall give a revised estimate of the time when they will be ready (and so on).
(2) Before providing any drugs or appliances in accordance with a prescription form or a repeatable prescription—
(a)the chemist shall ask any person who makes a declaration that the person named on the prescription form or the repeatable prescription does not have to pay the charges specified in regulation 3(1) or (1A) of the Charges Regulations by virtue of either—
(i)entitlement to exemption under regulation 8(1) of the Charges Regulations, or
(ii)entitlement to remission of such charges under regulation 4 of the Remission of Charges Regulations,
to produce satisfactory evidence of such entitlement, unless the declaration is in respect of entitlement to exemption by regulation 8(1) of the Charges Regulations or in respect of entitlement to remission by virtue of sub-paragraphs (e) to (k) of regulation 4(2) of the Remission of Charges Regulations, and at the time of the declaration the chemist already has such evidence available to him; and
(b)if no satisfactory evidence, as required by paragraph (a), is produced to the chemist, the chemist shall endorse the form on which the declaration is made to that effect.
8.—(1) Where a chemist is presented with a prescription form or a repeatable prescription, the chemist shall only provide the drugs or appliances so ordered—
(a)if the prescription form or repeatable prescription is duly signed and endorsed as described in paragraph 5(1) or (2); and
(b)in accordance with the order and any directions given by the prescriber on the prescription form or repeatable prescription,
subject to any regulations in force under the Weights and Measures Act 1985(13) and the following provisions of this Part.
(2) Drugs or appliances so ordered shall be provided either by or under the direct supervision of a pharmacist.
(3) Where the pharmacist referred to in sub-paragraph (2) is employed by a chemist, the pharmacist must not be someone—
(a)who—
(i)has been disqualified under section 46(2)(b) of the Act (or under any corresponding provision in force in Scotland or Northern Ireland) from inclusion in the pharmaceutical list of a Primary Care Trust (or, in Scotland, of a Health Board or, in Northern Ireland, of a Health and Social Services Board), and
(ii)is the subject of a declaration under section 46(2)(c) of the Act (or any corresponding provision in force in Scotland or Northern Ireland) that he is not fit to be engaged in any capacity in the provision of pharmaceutical services; or
(b)who is suspended.
(4) If the order is for an appliance of a type requiring measuring and fitting by the chemist (for example a truss), the chemist shall make all necessary arrangements—
(a)for measuring the person named the a prescription form or repeatable prescription for the appliance; and
(b)for fitting the appliance.
(5) If the order is for a drug or appliance included in the Drug Tariff, the British National Formulary (including any Appendix published as part of that Formulary), the Dental Practitioner’s Formulary, the European Pharmacopoeia or the British Pharmaceutical Codex, the drug or appliance provided shall comply with the standard or formula specified therein.
(6) If the order—
(a)is an order for a drug; but
(b)is not an order for a controlled drug within the meaning of the Misuse of Drugs Act 1971 other than a drug which is for the time being specified in Schedules 4 or 5 to the Misuse of Drugs Regulations 2001,
and does not prescribe its quantity, strength or dosage, a chemist may provide the drug in such strength and dosage as in the exercise of his professional skill, knowledge and care he considers to be appropriate and, subject to sub-paragraph (7), in such quantity as he considers to be appropriate for a course of treatment for a period not exceeding five days.
(7) Where an order to which sub-paragraph (6) applies is for—
(a)an oral contraceptive substance;
(c)a drug, which is available for supply as part of pharmaceutical services only together with one or more other drugs; or
(d)an antibiotic in a liquid form for oral administration in respect of which pharmaceutical considerations require its provision in an unopened package,
which is not available for provision as part of pharmaceutical services except in such packages that the minimum size available contains a quantity appropriate to a course of treatment for a period of more than 5 days, the chemist may provide the minimum size available package.
(8) Where any drug to which this paragraph applies (that is, a drug that is not one to which the Misuse of Drugs Act 1971 applies, unless it is a drug for the time being specified in Schedules 4 or 5 to the Misuse of Drugs Regulations 2001), ordered by a prescriber on a prescription form or repeatable prescription, is available for provision by a chemist in a pack in a quantity which is different to the quantity which has been so ordered, and that drug is—
(a)sterile;
(b)effervescent or hygroscopic;
(c)a liquid preparation for addition to bath water;
(d)a coal tar preparation;
(e)a viscous preparation; or
(f)packed at the time of its manufacture in a calendar pack or special container;
the chemist shall, subject to sub-paragraph (9), provide the drug in the pack whose quantity is nearest to the quantity which has been so ordered.
(9) A chemist shall not provide, pursuant to sub-paragraph (8), a drug in a calendar pack where, in his opinion, it was the intention of the prescriber who ordered the drug that it should be provided only in the exact quantity ordered.
(10) In this paragraph—
(a)“calendar pack” means a blister or strip pack showing the days of the week or month against each of the several units in the pack; and
(b)“special container” means any container with an integral means of application or from which it is not practicable to dispense an exact quantity.
(11) Except as provided in sub-paragraph (12), a chemist shall not provide a Scheduled drug in response to an order by name, formula or other description on a prescription form or repeatable prescription.
(12) Where a drug has an appropriate non-proprietary name and it is ordered on a prescription form or repeatable prescription either by that name or by its formula, a chemist may provide a drug which has the same specification notwithstanding that it is a Scheduled drug, provided that where a Scheduled drug is a pack which consists of a drug in more than one strength, such provision does not involve the supply of part only of the pack.
(13) Where a drug which is ordered as specified in sub-paragraph (12) combines more than one drug, that sub-paragraph shall apply only if the combination has an appropriate non-proprietary name, whether the individual drugs which it combines do so or not.
(14) A chemist shall provide any drug which he is required to provide under this paragraph in a suitable container.
9.—(1) A chemist may refuse to provide the drugs or appliances ordered on a prescription form or repeatable prescription where—
(a)the chemist reasonably believes that it is not a genuine order for the person named on the prescription form or the repeatable prescription (for example because he reasonably believes the form has been stolen or forged);
(b)it appears to the chemist that there is an error on the prescription form or on the repeatable prescription or its associated batch issue (including a clinical error made by the prescriber) or that, in the circumstances, providing the drugs or appliances would be contrary to the chemist’s clinical judgement;
(c)the chemist or other persons on the premises are subjected to or threatened with violence by the person presenting the prescription form or repeatable prescription, or by any person accompanying that person; or
(d)the person presenting the prescription form or repeatable prescription, or any other person accompanying that person, commits or threatens to commit a criminal offence.
(2) A chemist shall refuse to provide a drug ordered on a prescription form or repeatable prescription where the order is for a prescription only medicine which the prescriber was not entitled to prescribe.
(3) A chemist shall refuse to provide drugs or appliances ordered on a repeatable prescription where—
(a)he has no record of that prescription;
(b)he does not have any associate batch issue and it is not presented to him;
(c)it is not signed by a repeatable prescriber;
(d)to do so would not be in accordance with any intervals specified in the prescription;
(e)it would be the first time a drug or appliance had been provided pursuant to the prescription and the prescription was signed more than six months previously;
(f)if the repeatable prescription was signed more than one year previously;
(g)the expiry date on the repeatable prescription has passed; or
(h)where he has been informed by the repeatable prescriber that the prescription is no longer required.
(4) Where a patient requests the supply of drugs or appliances ordered on a repeatable prescription (other than on the first occasion that he makes such a request), a chemist shall only provide the drugs and appliances so ordered if he is satisfied—
(a)that the patient in respect of whom the prescription was written—
(i)is taking or using, and is likely to continue to take or use, the drug or appliance appropriately, and
(ii)is not suffering from any side effects of the treatment which indicates the need or desirability of reviewing the patient’s treatment;
(b)that the medication regimen of the patient in respect of whom the prescription was written has altered in a way which indicates the need or desirability of reviewing the patient’s treatment; and
(c)there have been no changes to the health of the patient in respect of whom the prescription was written which indicate the need or desirability of reviewing the patient’s treatment.
10. In connection with the services provided under paragraph 4, a chemist shall—
(a)ensure that appropriate advice is given to patients about any drugs or appliances provided to them—
(i)to enable them to utilise the drugs or appliances appropriately, and
(ii)to meet the patient’s reasonable needs for general information about the drugs or appliances;
(b)provide appropriate advice to persons to whom they provide drugs or appliances on—
(i)the safe keeping of the drugs or appliances, and
(ii)returning unwanted drugs or appliances to the pharmacy for safe destruction;
(c)provide appropriate advice to persons to whom they provide drugs or appliances in accordance with a repeatable prescription in particular on the importance of only requesting those items which they actually need;
(d)provide a patient with a written note of any drug or appliance which is owed, and inform the patient when the drug or appliance becomes available;
(e)keep and maintain records—
(i)of drugs and appliances provided, where it is necessary or desirable to do so in order to facilitate the continued care of the patient;
(ii)in appropriate cases, of advice given and any interventions or referrals made (in particular of clinically significant interventions in cases involving repeatable prescriptions), and
(iii)of notes provided under sub-paragraph (d);
(f)undertake appropriate training in respect of repeat prescribing, having regard to any recommendations in respect of such training set out in the Drug Tariff;
(g)if he takes possession of a repeatable prescription or an associated batch issue, securely store that repeatable prescription or associated batch issue;
(h)maintain records of repeatable prescriptions in such a form as to provide a clear audit trail of supplies under the repeatable prescription (including dates and quantities supplied);
(i)destroy any surplus batch issues relating to drugs or appliances—
(i)which are not required, or
(ii)where a patient is refused the drugs or appliances pursuant to paragraph 9;
(j)ensure that where a person is refused drugs or appliances pursuant to paragraphs 9(1)(b), (2), (3) or (4), the patient is referred back to the prescriber for further advice;
(k)where a patient is provided with drugs or appliances under a repeatable prescription, notify the prescriber of any clinically significant issues arising in connection with the prescription and keep a record of that notification; and
(l)notify the prescriber of any refusal to provide drugs or appliances pursuant to paragraph 9(4).
11. A chemist shall, to the extent paragraph 12 requires and in the manner described in that paragraph, accept and dispose of unwanted drugs presented to him for disposal.
12.—(1) Subject to paragraph (2), where a person presents to a chemist or any of his staff any drugs provided for a patient in, and which have been kept in—
(a)a private household; or
(b)a residential care home,
the chemist shall accept the drugs and dispose of them in accordance with sub-paragraph (3).
(2) A chemist shall not be required to accept any drugs for disposal unless the Local Health Board with which he is listed has made arrangements with the chemist for the collection and disposal of drugs of that description.
(3) On receipt of the drugs, the chemist shall—
(a)where required to do so by the Local Health Board or by a waste disposal contractor retained by the Local Health Board, separate solid drugs or ampoules, liquids and aerosols from each other;
(b)store the drugs in containers provided by the Local Health Board, or by a waste disposal contractor retained by the Local Health Board for the purpose of storing drugs of that description;
(c)comply with any other statutory requirements in respect of storing or the disposal of drugs of that description (meeting those requirements are therefore an essential service for the purposes of these Regulations),
and shall co-operate with any suitable arrangements that the Local Health Board has in place for regular collection of the drugs from his premises by or on behalf of the Local Health Board.
13. In connection with the services provided under paragraph 11, a chemist shall—
(a)ensure that he and any staff he has, are aware of the risks associated with the handling of waste drugs and the correct procedures to be used to minimise those risks; and
(b)ensure that he and any staff he has have readily available and close to any place where waste drugs are stored appropriate protective equipment, including gloves, overalls and materials to deal with spillages.
14. A chemist shall, to the extent paragraphs 15 and 16 require, and in the manner set out those paragraphs, promote public health messages to members of the public.
15.—(1) Where a person using a pharmacy—
(a)presents a prescription form or repeatable prescription to a chemist; and
(b)it appears to the chemist that the person—
(i)has diabetes,
(ii)is at risk of coronary heart disease or high blood pressure, or
(iii)smokes or is overweight,
the chemist shall, as appropriate, provide advice to that person with the aim of increasing that person’s knowledge and understanding of the health issues which are relevant to that person’s personal circumstances.
(2) Advice given under sub-paragraph (1) may be backed up, as appropriate—
(a)by the provision of written material (for example leaflets); and
(b)by referring the person to other sources of information or advice.
(3) A chemist shall, in appropriate cases, keep and maintain a record of advice given pursuant to this paragraph, and that record shall be in a form that facilitates—
(a)auditing of the provision of pharmaceutical services by the chemist; and
(b)follow-up care for the person who has been given the advice.
16. A chemist shall, at the request of his Local Health Board, ensure that—
(a)he and any staff he has participate, in the manner reasonably requested by his Local Health Board, in up to six campaigns in each calendar year to promote public health messages to users of his pharmacy; and
(b)where requested to do so by the Local Health Board, record the number of people to whom he or his staff have provided information as part of one of those campaigns.
17. A chemist shall, to the extent paragraph 18 requires and in the manner set out in that paragraph, provide information to users of his pharmacy about other health and social care providers and support organisations.
18.—(1) Where it appears to a chemist or his staff, having regard to the need to minimise inappropriate use of health and social care services and of support services, that a person using his pharmacy—
(a)requires advice, treatment or support that the chemist cannot provide; but
(b)another provider, of which the chemist is aware, of health or social care services or of support services is likely to be able to provide that advice, treatment or support,
the chemist shall provide contact details of that provider to that person and shall, in appropriate cases, refer that person to that provider.
(2) Where appropriate, a referral under sub-paragraph (1) may be made by means of a written referral note.
(3) The chemist shall, in appropriate cases, keep and maintain a record of any information given or referral made under sub-paragraph (1) and that record shall be in a form that facilitates—
(a)auditing of the provision of pharmaceutical services by the chemist; and
(b)follow-up care for the person who has been given the information or in respect of whom the referral has been made.
19. A chemist shall, to the extent paragraph 20 requires and in the manner set out in that paragraph, provide advice and support to people caring for themselves or their families.
20.—(1) Where it appears to a chemist or his staff, having regard to the need to minimise the inappropriate use of health and social care services, that a person using his pharmacy would benefit from advice from the chemist to help him manage a medical condition (including, in the case of a carer, to help the carer in assisting in the management of another person’s medical condition), the chemist shall provide advice to the person using the pharmacy as regards managing the medical condition, including as appropriate advice—
(a)on treatment options, including advice on the selection and use of appropriate drugs which are not prescription only medicines; and
(b)on changes to the patient’s lifestyle.
(2) The chemist shall, in appropriate cases, keep and maintain a record of any advice given under sub-paragraph (1) and that record shall be in a form that facilitates—
(a)auditing of the provision of pharmaceutical services by the chemist; and
(b)follow-up care for the person to whom or in respect of whom the advice has been given.
21.—(1) A chemist shall ensure that pharmaceutical services are provided at each of the premises from which he has undertaken to provide pharmaceutical services—
(a)for not less than 40 hours each week; or
(b)if his Local Health Board, or on appeal the National Assembly for Wales, has directed (either under this Part or on or before 31 March 2005) that he may provide pharmaceutical services at the premises for fewer than 40 hours per week, provided that he provides those services at set times and on set days, at the times and on the days so set;
(c)if his Local Health Board, or on appeal the National Assembly for Wales, has directed on or before 31 March 2005 that he must provide pharmaceutical services at the premises for more than 40 hours per week, at set times and on set days, at the times and on the days so set; or
(d)if his Local Health Board, or on appeal the National Assembly for Wales, has directed under this Part that he must provide pharmaceutical services at the premises for more than 40 hours per week—
(i)for the total number of hours each week required by virtue of that direction, and
(ii)as regards the additional hours for which he is required to provide pharmaceutical services by virtue of that direction, at the days on which and the times at which he is required to provide pharmaceutical services during those additional hours, as set out in that direction,
but a Local Health Board may, in appropriate circumstances, agree a temporary suspension of services for a set period, where it has received three months notice of the proposed suspension.
(2) At each of the premises from which a chemist has undertaken to provide pharmaceutical services, he shall exhibit—
(a)a notice specifying the times at which the premises are open for the provision of drugs and appliances; and
(b)at times when the premises are not open, a notice based on information provided by the Local Health Board, legible from outside the premises, specifying the addresses of other chemists, included in the pharmaceutical list and the times at which drugs and appliances may be obtained from those addresses.
(3) A chemist shall, on request, submit a return to the Local Health Board setting out—
(a)the times at which pharmaceutical services are provided at each of the premises from which he has undertaken to provide pharmaceutical services (including the times at which he is providing pharmaceutical services when he is not obliged to do so by virtue of sub-paragraph (1)); and
(b)the pharmaceutical services which he ordinarily provides at each of those premises,
but all chemists, if they are on a pharmaceutical list on 1 April 2005, shall supply such a return to the Local Health Board by 1 July 2005 and shall state in that return if the days and times submitted represent a change to the days on which and the times at which they provided pharmaceutical services at those premises prior to 1 April 2005.
(4) Where a chemist changes—
(a)the days on which or the times at which pharmaceutical services are to be provided at premises from which he has undertaken to provide pharmaceutical services; or
(b)the pharmaceutical services which he is ordinarily to provide at those premises,
he shall supply the Local Health Board with a return informing it of the change.
(5) Where a chemist has submitted a return under sub-paragraph (3) or (4) in respect of any premises, or where he has set out in an application under these Regulations for inclusion in the pharmaceutical list the days on which and the times at which pharmaceutical services will be provided at the premises to which the application relates if the application is granted—
(a)he shall ensure that pharmaceutical services are provided at the premises to which the return or application relates on the days and at the times set out in return or application (unless the return or application has been superseded by a return, or a further return, under sub-paragraph (4)); and
(b)he shall not change—
(i)the days on which or the times at which pharmaceutical services are to be provided at those premises; or
(ii)the pharmaceutical services which he is ordinarily to provide at those premises,
as set out in that return or application, for a period of at least three months after that return or application was received by the Local Health Board.
(6) Where a chemist is prevented by illness or other reasonable cause from complying with his obligations under sub-paragraph (1), he shall, where practicable, make arrangements with one or more chemists whose premises are situated in the neighbourhood for the provision of pharmaceutical services during that time.
(7) Where there is a temporary suspension in the provision of pharmaceutical services by a chemist for a reason beyond the control of the chemist, the chemist shall not be in breach of sub-paragraphs (1) and (2), provided that—
(a)he notifies the Local Health Board of that suspension as soon as practical; and
(b)he uses all reasonable endeavours to resume provision of pharmaceutical services as soon as practicable;
(8) Planned refurbishment of a pharmacy is neither a “reasonable cause” for the purposes of sub-paragraph (6) nor a “reason beyond the control of the chemist” for the purposes of sub-paragraph (7).
(9) For the purposes of calculating the number of hours that a pharmacy is open during a week that includes Christmas Day, Good Friday or a bank holiday, it shall be deemed that the pharmacy was open on that day at the times at which it would ordinarily have been open on that day of the week.
(10) In this Part —
the “additional hours” for which a chemist is to be required to provide pharmaceutical services are those hours during which the chemist would not be providing pharmaceutical services, were he subject to the condition set out in sub-paragraph (1)(a) and not the condition set out in sub-paragraph (1)(e); and
“existing direction” means one that has been made in accordance with this Part, or one that was in existence on 31 March 2005.
22.—(1) Where a Local Health Board issues a direction setting any times or days under this Part, it shall in doing so seek to ensure that the hours at which premises are open for the provision of pharmaceutical services are such as to ensure that the pharmaceutical services are provided on such days and at such times as are necessary to meet the needs of people in the neighbourhood, or other likely users of the pharmacy, for pharmaceutical services.
(2) In considering the matters mentioned in sub-paragraph (1) the Local Health Board may have regard to any pharmaceutical services that are being provided in that neighbourhood in circumstances where the chemist is not obliged to provide those services.
(3) The Local Health Board may only direct that a chemist may provide pharmaceutical services at premises for less than 40 hours in any week if it is satisfied that the provision of pharmaceutical services in the neighbourhood is likely to be adequate to meet the need for such services at times when the chemist is not providing pharmaceutical services.
(4) The Local Health Board may only direct that a chemist must provide pharmaceutical services at premises for more than 40 hours in any week where it is satisfied that he will receive reasonable remuneration in respect of the additional hours for which he is required to provide pharmaceutical services (and any additional remuneration payable under the Drug Tariff in respect of those hours is “reasonable remuneration” for these purposes”).
23.—(1) Where it appears to the Local Health Board, after consultation with or having considered the matter at the request of the Local Pharmaceutical Committee, that the times at which a pharmacy is or will be open for the provision of pharmaceutical services will not, or no longer meet, the needs of—
(a)people in the neighbourhood; or
(b)other likely users of his pharmacy,
for pharmaceutical services, it may carry out an assessment as to whether to issue a direction requiring the chemist whose pharmacy it is to provide pharmaceutical services at the pharmacy at set times and on set days (which may include Christmas Day, Good Friday and bank holidays).
(2) Before concluding the assessment under sub-paragraph (1) the Local Health Board shall—
(a)give notice to the chemist of any proposed changes to the times at which or the days on which the pharmacy is to be open; and
(b)allow him 30 days within which to make written representations to the Local Health Board about the proposed changes.
(3) After considering any representations made in accordance with sub-paragraph (2)(b), the Local Health Board shall—
(a)issue a direction (which will replace any existing direction) which meets the requirements of sub-paragraphs (4) and (5);
(b)confirm any existing direction setting the days on which and the times at which the chemist must provide pharmaceutical services at the pharmacy provided that the existing direction would meet the requirements of sub-paragraphs (4) and (5) if it were issued under this paragraph; or
(c)either—
(i)revoke (without replacing it) any existing direction setting the times at which or the days on which the chemist must provide pharmaceutical services at the pharmacy, or
(ii)in a case where there is no existing direction, issue no direction,
in which case, by virtue of paragraph 21(1)(a), the pharmacy will need to be open for not less than 40 hours each week.
(4) Where a Local Health Board issues a direction under sub-paragraph (3) in respect of a pharmacy that is required to be open—
(a)for more than 40 hours each week, it shall set out in that direction —
(i)the total number of hours each week for which the chemist shall provide pharmaceutical services at the pharmacy, and
(ii)as regards the additional hours for which he is to provide pharmaceutical services, the days on which and times at which he is required to provide those services during those additional hours,
but it shall not set out in that direction the days on which or the times at which he is to provide pharmaceutical services during hours which are not additional hours; or
(b)for less than 40 hours each week, it shall set out in that direction the days on which and times at which pharmaceutical services are to be provided at that pharmacy.
(5) The Local Health Board shall not issue a direction under sub-paragraph (3) that has the effect simply of requiring a pharmacy to be open for 40 hours each week on set days and at set times (that is, the direction must have the effect of requiring a pharmacy to be open for either more or less than 40 hours each week).
(6) The Local Health Board shall notify the chemist in writing of any direction issued or any other action taken under sub-paragraph (3), and where it sets new days on which or times at which the chemist is to provide pharmaceutical services at the pharmacy, it shall include with the notification a statement in writing of—
(a)the reasons for the change; and
(b)the chemist’s right of appeal under sub-paragraph (7).
(7) A chemist may, within 30 days of receiving notification under sub-paragraph (6) appeal in writing to the National Assembly for Wales against any direction issued or any other action taken under sub-paragraph (3) which sets new days on which or times at which the chemist is to provide pharmaceutical services.
(8) The National Assembly for Wales may, when determining an appeal, either confirm the action taken by the Local Health Board or take any action that the Local Health Board could have taken under sub-paragraph (3).
(9) The National Assembly for Wales shall notify the chemist in writing of its determination and shall in every case include with the notification a written statement of the reasons for the determination.
(10) If the times at which or the days on which a chemist is to provide pharmaceutical services at a pharmacy have been changed in accordance with this paragraph, the chemist shall introduce the changes—
(a)if he has not appealed under sub-paragraph (7), not later than 8 weeks after the date on which he receives his notification under sub-paragraph (6); or
(b)if he has appealed under sub-paragraph (7), not later than 8 weeks after the date on which he receives his notification under sub-paragraph (9).
24.—(1) A chemist may apply to a Local Health Board for it to change the days on which or the times at which he is obliged to provide pharmaceutical services at his pharmacy in a way that—
(a)reduces the total number of hours for which the chemist is obliged to provide pharmaceutical services each week; or
(b)keeps the total number of hours the same.
(2) Where a chemist makes an application under paragraph (1), as part of that application he shall provide the Local Health Board with such information as the Local Health Board may reasonably request in respect of any changes to the needs of the people in the neighbourhood, or other likely users of the pharmacy, for pharmaceutical services that are material to the application.
(3) The Local Health Board shall determine an application under sub-paragraph (1) within 60 days of receiving it (including any information required of the applicant in accordance with sub-paragraph (2).
(4) In determining the application, the Local Health Board shall—
(a)issue a direction (which will replace any existing direction) which meets the requirements of sub-paragraphs (5) and (6) and which has the effect of either granting the application under this paragraph or granting it only in part;
(b)confirm any existing direction setting the days on which and the times at which the chemist must provide pharmaceutical services at the pharmacy provided that the existing direction would meet the requirements of sub-paragraphs (5) and (6);
(c)either—
(i)revoke (without replacing it) any existing direction in respect of the times at which or the days on which the chemist must provide pharmaceutical services at the pharmacy, where this has the effect of granting the application under this paragraph or granting it only in part, or
(ii)in a case where there is no existing direction, issue no direction,
in which case, by virtue of paragraph 21(1)(a), the pharmacy will need to be open for not less than 40 hours each week.
(5) Where a Local Health Board issues a direction under sub-paragraph (4) in respect of a pharmacy that is required to be open—
(a)for more than 40 hours each week, it shall set out in that direction—
(i)the total number of hours each week for which the chemist shall provide pharmaceutical services at the pharmacy, and
(ii)as regards the additional hours for which he is to provide pharmaceutical services, the days on which and the times at which he is required to provide those services during those additional hours,
but it shall not set out in that direction the days on which or the times at which he is to provide pharmaceutical services during hours which are not additional hours; or
(b)for less than 40 hours each week, it shall set out in that direction the days on which and the times at which pharmaceutical services are to be provided at that pharmacy.
(6) The Local Health Board shall not issue a direction under sub-paragraph (4) that has the effect simply of requiring a pharmacy to be open for 40 hours each week no set days and at set times (that is, the direction must have the effect of requiring a pharmacy to be open for either more or less than 40 hours each week).
(7) Where the Local Health Board is considering taking action under sub-paragraph (4)(a) or sub-paragraph (4)(c)(i), it shall consult the Local Pharmaceutical Committee before determining the application.
(8) A Local Health Board shall notify the chemist in writing of any direction issued or any other action taken under sub-paragraph (4), and where this has the effect of refusing an application under this paragraph or granting it in part, it shall send the chemist a statement in writing setting out—
(a)the reasons for the refusal or, as the case may be, for granting the application only in part; and
(b)the chemist’s right of appeal under sub-paragraph (9).
(9) A chemist may, within 30 days of receiving a notification pursuant to sub-paragraph (8), appeal in writing to the National Assembly for Wales against any action under sub-paragraph (4) which has the effect of refusing an application under this paragraph or granting it only in part.
(10) The National Assembly for Wales may, when determining an appeal, either confirm the action taken by the Local Health Board or take any action that the Local Health Board could have taken under sub-paragraph (4).
(11) The National Assembly for Wales shall notify the chemist in writing of its determination and shall in every case include with the notification a written statement of the reasons for the determination.
(12) If the days on which or times at which a chemist is to provide pharmaceutical services at a pharmacy have been changed in accordance with this paragraph, the chemist shall introduce the changes—
(a)if he has not appealed under sub-paragraph (9), not earlier that 30 days after the date on which he receives his notification under sub-paragraph (8); or
(b)if he has appealed under sub-paragraph (9), not earlier than 30 days after the date on which he receives his notification under sub-paragraph (11).
(13) Where an application under sub-paragraph (1)—
(a)is received by 1 July 2005; and
(b)is in respect of a direction that was in existence on 31 March 2005 to require the applicant to provide pharmaceutical services at a pharmacy for more than 40 hours per week, and at set times and on set days,
if the Local Health Board fails to determine the application within 60 days of receiving it, in accordance with sub-paragraph (3), that application shall be deemed to have been granted, as from three months from the date on which the application was received by the Local Health Board.
(14) Where an application under sub-paragraph (1)—
(a)is received by 1 July 2005; and
(b)is in respect of a direction that was in existence on 31 March 2005 to require the applicant to provide pharmaceutical services at a pharmacy for more than 40 hours per week, and at set times and on set days,
until that application (including any appeal) is determined or deemed to have been granted, paragraph 22(1)(a) shall apply in respect in respect of the application as if for “40” there were substituted “30”.
25.—(1) A chemist shall, in connection with all the pharmaceutical services provided by him, participate, in the manner reasonably required by his Local Health Board, in an acceptable system of clinical governance.
(2) For these purposes a system of clinical governance is “acceptable” if it is considered acceptable by the National Assembly for Wales and comprises the following components—
(a)a patient and public involvement programme, which includes—
(i)a requirement that the chemist should produce in an approved manner, and make available in an appropriate manner, a practice leaflet in respect of his pharmacy,
(ii)a requirement that the chemist publicises the NHS services that are available at or from his pharmacy,
(iii)a requirement that the chemist should undertake an approved patient satisfaction survey annually, in an approved manner,
(iv)monitoring arrangements for drugs or appliances owed to patients but which are out of stock,
(v)an approved complaints system (which meets the requirements of this Part),
(vi)a requirement that the chemist co-operates appropriately with Local Community Health Council visits and takes appropriate action following the outcome of such visits,
(vii)a requirement that the chemist co-operates appropriately with any reasonable inspection or review that the Local Health Board or any relevant statutory authority wishes to undertake, and
(viii)monitoring arrangements for compliance with the Disability Discrimination Act 1995(14);
(b)a clinical audit programme (normally of five days), which includes at least one pharmacy-based audit and one multi-disciplinary audit agreed by his Local Health Board in each financial year;
(c)a risk management programme, which includes—
(i)arrangements for ensuring that all stock are handled in an appropriate way,
(ii)arrangements for ensuring that all equipment used in the provision of pharmaceutical services is maintained appropriately,
(iii)an approved incident reporting system, together with arrangements for analysing and responding to critical incidents,
(iv)appropriate standard operating procedures, including standard operating procedures in respect of repeatable prescriptions and providing advice and support to people caring for themselves or their families,
(v)appropriate waste disposal arrangements (in addition to those required under paragraphs 12 and 13) for clinical and confidential waste,
(vi)a clinical governance lead person in respect of each pharmacy,
(vii)appropriate child protection procedures, and
(viii)monitoring arrangements for compliance with the Health and Safety Act 1974;
(d)a clinical effectiveness programme, which includes arrangements for monitoring the effectiveness of the advice given by a chemist in respect of repeatable prescriptions or to people caring for themselves or their families;
(e)a staffing and staff management programme, which includes—
(i)arrangement for appropriate induction training for staff and locums,
(ii)appropriate training for all staff in respect of any role they are asked to perform,
(iii)arrangements for the checking of qualifications and references of all staff engaged in the provision of NHS services,
(iv)arrangements for identifying and supporting the development needs of all staff engaged in the provision of services as part of the health service including continuing professional development for registered chemists and any necessary accreditation in respect of the provision of directed services , and
(v)arrangements for addressing poor performance (in conjunction with a Local Health Board as appropriate);
(f)a use of information programme, which includes—
(i)appropriate arrangements (having regard to issues both of rights of access to information and of confidentiality) to support both health care delivery and clinical governance,
(ii)the chemist’s monitoring arrangements in respect of his compliance with the Data Protection Act 1998 and with regard to patient confidentiality, and
(iii)appropriate training for staff with regard to compliance with the Data Protection Act 1998 and patient confidentiality,
and for the purposes of this sub-paragraph “approved” means approved by the National Assembly for Wales.
26. A chemist shall provide pharmaceutical services and exercise any professional judgment in connection with the provision of such services in conformity with the standards generally accepted in the pharmaceutical profession.
27.—(1) A chemist or his staff shall not give, promise or offer to any person any gift or reward (whether by way of a share of or dividend on the profits of the business or by way of discount or rebate or otherwise) as an inducement to or in consideration of his presenting an order for drugs or appliances on a prescription form or repeatable prescription.
(2) Promising, offering or providing a compliance aid or a home delivery service is not a gift or reward for the purposes of sub-paragraph (1).
28. A chemist shall have in place arrangements for the handling and consideration of complaints about any matter connected with his provision of pharmaceutical services which shall—
(a)until the coming into force of regulations in relation to complaints about pharmaceutical services made under section 113 of the Health and Social Care (Community Health and Standards) Act 2003(15)?) (complaints about health care) comply with the provisions of paragraphs 10A and 10B of Schedule 2 to these Regulations as they apply on 31 March 2005; and
(b)upon the coming into force of such regulations, comply with those regulations.
29. A chemist with whom a Local Health Board makes an arrangement for the provision of any directed services shall comply with the terms and conditions of the arrangement.
30—(1) A chemist shall give notice to the Local Health Board within 28 days (or if this is impracticable, as soon as practicable thereafter) of—
(a)any occurrence requiring a change in the information recorded about him in the pharmaceutical list which he has not otherwise notified in accordance with these Regulations;
(b)in the case of a chemist who is an individual, any change of his private address; and
(c)in the case of a chemist that is a body corporate, any change to the address of its registered office.
(2) A chemist shall give the Local Health Board, if it so requests, the name of any pharmacist employed by him who is responsible for dispensing a particular prescription.
(3) Subject to sub-paragraph (7), a chemist that is a body corporate shall (if it is on a pharmaceutical list on 1 April 2005, by 1 July 2005) supply to its Local Health Board in writing the name and address of each of its directors and superintendent, and any changes to the names and addresses of each of its directors and superintendent.
(4) Subject to sub-paragraph (7), if a chemist or the director or superintendent of a chemist that is a body corporate is himself on, or is a director or superintendent of a body corporate which is on, another NHS performers or providers list (that is, on a list other than the pharmaceutical list referred to in sub-paragraph (1)), that person shall supply in writing to the Local Health Board —
(a)if he is a director or superintendent of a body corporate, the name and registered office of the body corporate on the other NHS performers or providers list; and
(b)particulars of the other NHS performers or providers list.
(5) Subject to sub-paragraph (7), if a chemist or the director or superintendent of a chemist that is a body corporate has himself in the five years prior to 1 April 2005 been on, or has in the five years prior to 1 April 2005 been the director or superintendent of a corporate body that which was when he was a director on, another NHS performers or providers list (that is, on a list other than the pharmaceutical list referred to in sub-paragraph (1)), that person shall supply in writing to the Local Health Board—
(a)the name and registered office of the body corporate on the other NHS performers or providers list; and
(b)particulars of the NHS performers or providers list.
unless that information has already been supplied pursuant to sub-paragraph (4).
(6) Subject to sub-paragraph (7), if a chemist or the director or superintendent of a chemist that is a body corporate shall inform the Local Health Board—
(a)if he, or a body corporate of which he is a director or superintendent, applies to be included in any of another Local Health Board’s NHS performers or providers lists, and of the outcome of any such application; and
(b)if he becomes a director or superintendent of a body corporate which is on any of another Local Health Board’s NHS performers or providers list, or which applies to be included in such a list, and the outcome of any such application.
(7) Where a chemist is a body corporate with a registered office in Wales, the information to be provided under sub-paragraphs (3) to (6) may be provided only to the Local Health Board in which that registered office is located, if the chemist also provides that Local Health Board with details of all the other Local Health Boards on whose pharmaceutical lists it is, and in these circumstances that Local Health Board shall pass the information on to any other Local Health Board —
(a)on whose pharmaceutical list the chemist is; or
(b)to whom the chemist makes an application to be on its pharmaceutical list,
that requests it.
(8) In this paragraph, “NHS performers or providers list” means—
(a)a pharmaceutical list; or
(b)any other list.
31. Where a chemist intends to withdraw from the pharmaceutical list, he shall notify the Local Health Board of this at least three months in advance of that date, unless it is impracticable for him to do so in which case he shall notify the Local Health Board as soon as it is practicable for him to do so.
32.—(1) Subject to regulations made under section 77 of the Act, all drugs, containers and appliances provided under these terms of service shall be provided free of charge.
(2) Where a chemist supplies a container in response to an order for drugs signed by a prescriber, or supplies an oxygen container or oxygen equipment, other than equipment specified in the Drug Tariff as not returnable to the chemist, the container and equipment shall remain the property of the chemist.
(3) Where any person who is entitled to a repayment of any charge paid under the Charges Regulations presents a chemist with a valid claim for repayment, the chemist shall make the repayment.
(4) For the purposes of sub-paragraph (3), a claim for repayment is only valid if—
(a)until 30 June 2005, it is duly made on Form WP57 0403 within three months of the date on which the charge was paid; or
(b)from 1 July 2005, it is duly made on Form WP57 0405 within three months of the date on which the charge was paid.
33.—(1) A chemist shall allow persons authorised in writing by the Local Health Board to enter and inspect his pharmacy at any reasonable time, for the purposes of—
(a)ascertaining whether or not the chemist is complying with the requirements of this Schedule;
(b)auditing, monitoring and analysing—
(i)the provision made by the chemist for patient care and treatment, and
(ii)the management by the chemist of the pharmaceutical services he provides,
where the conditions in sub-paragraph (2) are satisfied.
(2) The conditions are that—
(a)reasonable notice of the intended entry has been given;
(b)the Local Pharmaceutical Committee for the area where the pharmacy is situated have been invited to be present at the inspection, where this is requested by the chemist;
(c)the person authorised in writing carries written evidence of his authorisation, which he produces on request; and
(d)he does not enter any part of the premises used solely as residential accommodation without the consent of the resident.
(3) A chemist shall, at the request of the Local Health Board or of person authorised in writing mentioned in sub-paragraph (1), allow it or him access to any information which it or he reasonably requires—
(a)for the purposes mentioned in sub-paragraph (1); or
(b)in the case of the Local Health Board, in connection with its functions that relate to pharmaceutical services.”.
9. For Part III of Schedule 2 to the principal Regulations (Terms of Service for Doctors who Provide Pharmaceutical Services) substitute the following—
34.—(1) Subject to the following provisions of this Part, where a patient presents on a prescription form—
(a)an order for drugs, not being Scheduled drugs, or for appliances, not being restricted availability appliances, signed by an independent prescriber;
(b)an order for drugs specified in Schedule 2 to the Prescription of Drugs Regulations, signed by, and endorsed on its face with the reference “SLS” by an independent prescriber; or
(c)an order for restricted availability appliances, signed by and endorsed on its face with the reference “SLS” by an independent prescriber,
to a doctor who is authorised or required by regulation 20 to provide the drugs or appliances to that patient, the doctor may provide to the patient such of the drugs or appliances so ordered as he supplies in the normal course of his practice.
(2) Drugs and listed appliances provided under this paragraph shall be provided in a suitable container.
(3) In this Part “independent prescriber” means a prescriber other than the doctor who is authorised or required by a Local Health Board to provide drugs or appliances in accordance with regulation 20.
35. In circumstances where paragraph 34 does not apply and subject to the following provisions of this Part, where a doctor is authorised or required by a Local Health Board under regulation 20 to provide drugs of appliances to a patient—
(a)he shall record an order for the provision of any drugs, or appliances which are needed for the treatment of the patient on a prescription form completed in accordance with the term of a contract which gives effect to paragraph 39(3) of Schedule 6 to the GMS Regulations or an equivalent provision applying in relation to that contract;
(b)he shall provide those drugs and appliances in a suitable container;
(c)he shall provide for the patient a drug specified in Schedule 2 to the Prescription of Drugs Regulations only where the conditions in paragraph 42(2) of Schedule 6 to the GMS Regulations are satisfied;
(d)he shall provide for the patient a restricted availability appliance only if the patient is a person, or it is for a purpose, specified in the Drug Tariff.
36. Before providing the drugs or listed appliances recorded on a prescription form in accordance with paragraph 34(1), or the drugs or medicines or listed appliances ordered on a prescription form in accordance with paragraph 35(a), a doctor who is authorised or required by the Local Health Board under regulation 20 to provide drugs and appliances to a patient shall—
(a)ask any person who makes a declaration on the prescription form that the patient does not have to pay the charges specified in regulation 4(1) of the Charges Regulations by virtue of either—
(i)entitlement to exemption under regulation 8(1) of the Charges Regulations, or
(ii)entitlement to remission of such charges under regulation 4 of the Remission of Charges Regulations,
to produce satisfactory evidence of such entitlement unless the declaration in respect of entitlement to exemption by virtue of regulation 8(1) of the Charges Regulations or in respect of entitlement to remission by virtue of regulation 4(2)(e) to (k) of the Remission of Charges Regulations, and at the time of the declaration the doctor already has such evidence available to him; and
(b)if no satisfactory evidence, as required by sub-paragraph (a) is produced to him (and, where it is relevant, none is already available), the doctor shall endorse the form on which the declaration is made to that effect.
37.—(1) Subject to sub-paragraph (2), a doctor who is authorised or required by a Local Health Board under regulation 20 to provide drugs or appliances to a patient shall not provide for a patient any Scheduled drug, except that, where he has ordered a drug which has an appropriate non-proprietary name either by the name or by its formula, he may provide a drug which has the same specification notwithstanding that it is Scheduled drug (but, in the case of a drug which combines more than one drug, only if the combination has an appropriate non-proprietary name).
(2) Nothing in this paragraph or paragraph 36 shall prevent a doctor providing, otherwise than under pharmaceutical services, a Scheduled drug or a restricted availability appliance for a patient.
38.—(1) The terms of a GMS contract giving effect to regulation 24 of, and Schedule 5 to the GMS Regulations (fees and charges) apply in respect of the provision of any drugs or appliances by a doctor as they apply in respect of prescriptions for drugs and appliances.
(2) Where a doctor who is authorised or required by a Local Health Board under regulation 20 to provide drugs or appliances under pharmaceutical services—
(a)in accordance with this Part; and
(b)had the drug or appliance been provided by a contractor providing dispensing services under a GMS contract, the contractor would have been entitled to a payment in respect of the drug or appliance by virtue of directions given by the National Assembly for Wales under section 28T of the Act,
the Local Health Board shall credit him with the payment.
39.—(1) Where a doctor who is authorised or required by a Local Health Board under regulation 20 to provide drugs or appliances to a patient, or who otherwise provides pharmaceutical services, is a GMS contractor, or is engaged or employed by a GMS contractor, the complaints procedure established in accordance with the terms of a GMS contract which gives effect to paragraph 90 of Schedule 6 to the GMS Regulations shall apply in relation to any matter reasonably connected with his provision of pharmaceutical services as it applies as respect to services provided under that contract or agreement.
(2) Accordingly, the term of the GMS contract which gives effect to paragraph 95 of Schedule 6 to the GMS Regulations also applies in relation to complaints about such matters.”.
10. For paragraph 6 of Schedule 3 to the principal Regulations (Application for Inclusion in a Pharmaceutical List or Inclusion in a List in Respect of Different Services or Premises) substitute—
“6. (To be completed by all applicants)
Available | Proposed | |
---|---|---|
Clinical Governance and CPD | □ | □ |
Dispensing (including repeat dispensing and compliance aids required under the Disability Discrimination Act) | □ | □ |
Disposal of unwanted medicines | □ | □ |
Promotion of healthy lifestyles | □ | □ |
Sign-posting patients to other NHS services | □ | □ |
Support for self-care | □ | □ |
Available | Proposed | |
---|---|---|
Medicines Use Review | □ | □ |
Prescription Linked Intervention | □ | □ .”. |
11.—(1) For the purposes of this regulation, a reference to a numbered paragraph is a reference to a paragraph bearing that number in Schedule 2 to the principal Regulations as they were in force on 31 March 2005.
(2) Any determination or direction made—
(a)by a Local Health Board; or
(b)on appeal, by the National Assembly for Wales,
in accordance with paragraph 4 concerning the days on which and the times at which a chemist is to provide pharmaceutical services that is in existence on 31 March 2005 will remain in existence until a subsequent determination or direction is made in accordance with the provisions substituted by regulation 8 of these Regulations.
(3) Where before 1 April 2005—
(a)a complaint has been made in accordance with the provisions of paragraphs 10A and 10B; or
(b)in accordance with the provisions of paragraph 4—
(i)an application has been made by a chemist to a Local Health Board, or
(ii)a review or variation has been initiated by a Local Health Board, or
(iii)an appeal has been made to the National Assembly for Wales,
concerning the times at which a chemist is to provide pharmaceutical services,
the provisions of these paragraphs shall (notwithstanding the coming into force of the substitution made by regulation 8 of these Regulations) continue to apply on and after that date to any investigation, consideration , application, approval, variation, review or appeal which, by virtue of these paragraphs, falls to be undertaken, held or made in relation to any such complaint, application, variation, review or appeal.
12. A chemist who is providing pharmaceutical services on 31 March 2005 by virtue of a particular entry on a pharmaceutical list when he provides pharmaceutical services pursuant to that entry, need not comply with the terms of service that are substituted into Schedule 2 to the principal Regulations by regulation 8, apart from Part 3, until 1 October 2005, provided that until that date he complies in addition with the terms of service as set out in Parts I and II of Schedule 2 to the principal Regulations as they apply on 31 March 2005, apart from paragraph 4 of that Schedule.
Signed on behalf of the National Assembly for Wales under section 66(1) of the Government of Wales Act1998 (16).
D. Elis-Thomas
The Presiding Officer of the National Assembly
31 March 2005
(This note is not part of the Regulations)
These Regulations further amend the National Health Service (Pharmaceutical Services) Regulations 1992 (S.I.1992/662) (“the principal Regulations”) which govern the arrangements the provision of pharmaceutical services under the National Health Service Act 1977.
The amendments made by these Regulations introduce a contractual framework for the provision of pharmaceutical services which will enable pharmacies to provide a greater range of services and to be rewarded for the range and quality of those services.
Regulation 8 of these Regulations replaces Part II of the Terms of Service for Chemists which are contained within Schedule 2 to the principal Regulations with new terms of service for Chemists which are contained within Parts 2 to 5 of the substituted provision. The new terms of service introduce three tiers of pharmaceutical services: firstly, nationally set essential services, which include dispensing, repeat dispensing, clinical governance requirements and disposal of medication; secondly, advanced services, which are also nationally set and which currently comprise medicines use review and prescription intervention services; and finally, locally enhanced services, which can commissioned by Local Health Boards and the terms of which can be agreed locally.
Regulation 9 substitutes a new Part 6 into Schedule 2 to the principal Regulations. This replaces, without change, the terms of services for doctors who provide pharmaceutical services.
These Regulations make other amendments to the principal Regulations that are consequential upon the introduction of the new contractual framework for chemists.
Regulations 11 and 12 contain transitional provisions.
1977 c. 49; Section 41 was substituted by the Health and Social Care Act 2001 (c. 15) (“the 2001 Act”), section 42(1); and amended by the National Health Service Reform and Healthcare Professions Act 2002 (c. 17) (“the 2002 Act”), Schedule 2, paragraph 13 and by the Health and Social Care (Community Health and Standards) Act 2003 (c. 43) (“the 2003 Act”).
Section 42 was substituted by the National Health Service (Amendment) Act 1986 (c. 66), section 3(1); extended by the Health and Medicines Act 1988 (c. 49), section 17; and amended by SI 1987/2202, article 4; by the National Health Service and Community Care Act 1990 (c. 19) (“the 1990 Act”), section 12(3) and by the Health Authorities 1995 (c. 17) (“the 1995 Act”), Schedule 1, paragraph 30; by the 2001 Act, sections 20(6), 23(5), 40(3), 43(2), (3) and (4) and by Schedule 6, Part 1; and by the 2002 Act, Schedule 2, paragraph 16.
Section 43 was amended by the Health Services Act 1980 (c. 53), Schedule 9, paragraph 18(2); by the 1995 Act, Schedule 1, paragraph 31; by the Pharmacists (Fitness to Practise) Act 1997 (c. 19), paragraph 6 of the Schedule; and by the National Health Service (Primary Care) Act 1997, section 29(1) and Schedule 2, paragraph 14; by the 1990 Act, Schedule 9, paragraph 18(2); by the 2001 Act, sections 20(7), 42(2) and 43(5); by the 2002 Act Schedule 2, paragraph 17; and by the 2003 Act, Schedule 11, paragraph 19.
See section 128(1) as amended by the 1990 Act, section 26(2)(g) and (i), and by the Health Act 1999 (c. 8) (“the 1999 Act), Schedule 4, paragraph 38(2)(b), for the definitions of “prescribed” and “regulations”.
Section 126(4) was amended by the 1990 Act, section 65(2) and the 1999 Act , Schedule 4, paragraph 37(6).
The functions of the Secretary of State under sections 41, 42, 43, and 126(4) of the National Health Service Act 1977 were transferred to the National Assembly for Wales by the National Assembly for Wales (Transfer of Functions) Order 1999, S.I.1999/672, article 2 and Schedule 1, as amended by the 1999 Act, section 66(5), the Health and Social Care Act 2001 (c. 15), section 68(1), National Health Service Reform and Health Care Professions Act 2002 (c. 17), section 40(1) and the Health and Social Care (Community Health and Standards) Act 2003 (c. 43), section 197(1).
The register is maintained by the Health Professions Council in accordance with Article 6 of the Health Professions Order 2002 (SI 2002/254)
Sections 49I and 49J of the National Health Service Act 1977 (c. 49) (“the Act”) were inserted by the Health and Social Care Act 2001 (c. 15) (“the 2001 Act), section 25; and amended by the National Health Service Reform and Healthcare Professions Act 2002 (c. 17) (“the 2002 Act”), section 2(5) and Schedule 2. Section 49I was also amended by the 2003 Health and Social Care (Community Health and Standards) Act 2003 (c. 43) (“the 2003 Act”), section 196 and Schedule 14.
Section 28DA was inserted into the Act by the National Health Service (Primary Care) Act 1997, section 21(1); and was amended by the 2002 Act, section 42 and Schedule 3; and by the 2003 Act, section 184 and Schedule 11.
Section 43D was inserted by section 24 of the 2001 Act; was amended by section 2(5 ) of and Schedule 2 to the 2002 Act and by section 196 of and Schedule 14 to the 2003 Act.
Inserted by the 2001 Act, section 26(2), repealed in relation to personal medical services by the 2003 Act, sections 178, 196 and Schedule 14.
S.I. 2004/905 (W.89)