- Y Diweddaraf sydd Ar Gael (Diwygiedig)
- Gwreiddiol (Fel y'i Deddfwyd)
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There are currently no known outstanding effects for the Health Service Medical Supplies (Costs) Act 2017.
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An Act to make provision in connection with controlling the cost of health service medicines and other medical supplies; to make provision in connection with the provision of pricing and other information by those manufacturing, distributing or supplying those medicines and supplies, and other related products, and the disclosure of that information; and for connected purposes.
[27th April 2017]
Be it enacted by the Queen's most Excellent Majesty, by and with the advice and consent of the Lords Spiritual and Temporal, and Commons, in this present Parliament assembled, and by the authority of the same, as follows:—
In section 164 of the National Health Service Act 2006 (remuneration for persons providing pharmaceutical services), after subsection (8) insert—
“(8A)Regulations may impose requirements in relation to remuneration in respect of special medicinal products.
(8B)Such regulations may, for example, require determining authorities to ensure—
(a)that remuneration is to be calculated by reference to the outcome of prescribed procedures, or
(b)that determinations do not provide for or permit remuneration to be paid in prescribed circumstances.
(8C)Procedures prescribed by virtue of subsection (8B)(a) may include the person to whom remuneration is payable, a health service body or a determining authority—
(a)carrying out inquiries to ensure that remuneration is reasonable, or
(b)estimating an amount of remuneration that is reasonable (whether or not the estimated amount corresponds exactly to expenses in respect of which remuneration is to be paid).
(8D)Circumstances prescribed by virtue of subsection (8B)(b) may include circumstances in which special medicinal products are made available to persons who provide pharmaceutical services under this Part—
(a)by a health service body, or
(b)under an arrangement for the supply of special medicinal products to which a health service body is a party.
(8E)In subsections (8A) to (8D)—
“health service body” has the meaning given by section 9(4);
“special medicinal product” means a product which is a special medicinal product for the purposes of regulation 167 of the Human Medicines Regulations 2012 (S.I. 2012/1916).”
Commencement Information
I1S. 1 in force at 7.8.2017 by S.I. 2017/809, reg. 2(a)
In section 88 of the National Health Service (Wales) Act 2006 (remuneration for persons providing pharmaceutical services), after subsection (8) insert—
“(8A)Regulations may impose requirements in relation to remuneration in respect of special medicinal products.
(8B)Such regulations may, for example, require determining authorities to ensure—
(a)that remuneration is to be calculated by reference to the outcome of prescribed procedures, or
(b)that determinations do not provide for or permit remuneration to be paid in prescribed circumstances.
(8C)Procedures prescribed by virtue of subsection (8B)(a) may include the person to whom remuneration is payable, a health service body or a determining authority—
(a)carrying out inquiries to ensure that remuneration is reasonable, or
(b)estimating an amount of remuneration that is reasonable (whether or not the estimated amount corresponds exactly to expenses in respect of which remuneration is to be paid).
(8D)Circumstances prescribed by virtue of subsection (8B)(b) may include circumstances in which special medicinal products are made available to persons who provide pharmaceutical services under this Part—
(a)by a health service body, or
(b)under an arrangement for the supply of special medicinal products to which a health service body is a party.
(8E)In subsections (8A) to (8D)—
“health service body” has the meaning given by section 7(4);
“special medicinal product” means a product which is a special medicinal product for the purposes of regulation 167 of the Human Medicines Regulations 2012 (S.I. 2012/1916).”
Commencement Information
I2S. 2 in force at 21.11.2022 by S.I. 2022/1201, art. 2
(1)Section 261 of the National Health Service Act 2006 (voluntary schemes for controlling the cost of health service medicines) is amended as follows.
(2)In subsection (1)—
(a)for “and 263” substitute “ , 263 and 264A ”,
(b)for “the purpose of” substitute “ one or more of the following purposes ”,
(c)omit the “or” before paragraph (b), and
(d)after paragraph (b) insert—
“(c)providing for any manufacturer or supplier to whom the scheme relates to pay to the Secretary of State an amount calculated by reference to sales or estimated sales of any health service medicines (whether on the basis of net prices, average selling prices or otherwise).”
(3)In subsection (4) for “either” substitute “ any ”.
(4)After subsection (8) insert—
“(9)The Secretary of State may provide for any amount payable in accordance with a voluntary scheme by any manufacturer or supplier to whom the scheme applies to be paid to the Secretary of State within a specified period.
(10)Neither of the following affects any liability of a manufacturer or supplier to pay amounts to the Secretary of State arising during a period when a health service medicine was covered by a voluntary scheme treated as applying to the person or the taking of any action in relation to any such liability—
(a)the withdrawal of consent by the person to the scheme being treated as applying to the person;
(b)the giving of notice to the person under subsection (4).”
Commencement Information
I3S. 3 in force at 7.8.2017 by S.I. 2017/809, reg. 2(b)
For section 262(2) of the National Health Service Act 2006 (circumstances in which powers not exercisable) substitute—
“(2)If at any time a health service medicine is covered by a voluntary scheme applying to its manufacturer or supplier, the powers conferred by this section may not be exercised at that time in relation to that manufacturer or supplier as regards that medicine.”
Commencement Information
I4S. 4 in force at 7.8.2017 by S.I. 2017/809, reg. 2(c)
(1)Section 263 of the National Health Service Act 2006 (statutory schemes for controlling the cost of health service medicines) is amended as follows.
(2)In subsection (1)—
(a)after “body” insert “ and any other person the Secretary of State thinks appropriate ”,
(b)for “the purpose of” substitute “ one or more of the following purposes ”,
(c)omit the “or” before paragraph (b), and
(d)after paragraph (b) insert—
“(c)providing for any manufacturer or supplier of any health service medicines to pay to the Secretary of State an amount calculated by reference to sales or estimated sales of those medicines (whether on the basis of net prices, average selling prices or otherwise).”
(3)After subsection (1) insert—
“(1A)Consultation about the proposed exercise of a power under subsection (1) must include consultation about the following—
(a)the economic consequences for the life sciences industry in the United Kingdom;
(b)the consequences for the economy of the United Kingdom;
(c)the consequences for patients to whom any health service medicines are to be supplied and for other health service patients.”
(4)After subsection (5) insert—
“(5A)The scheme may provide for any amount payable in accordance with the scheme by any manufacturer or supplier to whom the scheme applies to be paid to the Secretary of State within a specified period.”
(5)For subsection (7) substitute—
“(7)If at any time a health service medicine is covered by a voluntary scheme applying to its manufacturer or supplier, the powers conferred by this section may not be exercised at that time in relation to that manufacturer or supplier as regards that medicine.”
(6)After subsection (7) insert—
“(8)Subsection (7) does not affect any liability of a person to pay amounts to the Secretary of State arising during a period when a health service medicine was covered by a statutory scheme applying to the person or the taking of any action in relation to any such liability.”
Commencement Information
I5S. 5 in force at 7.8.2017 by S.I. 2017/809, reg. 2(d)
(1)The National Health Service Act 2006 is amended as follows.
(2)Section 265 (enforcement) is amended as follows.
(3)In subsection (4)—
(a)after “261(8)(b)” insert “ or (9) ”, and
(b)after “section 263(4), (5)” insert “ , (5A) ”.
(4)After subsection (8) insert—
“(8A)Subsection (8) does not apply to any action by the Secretary of State to recover as a debt any amount required to be paid to the Secretary of State by virtue of any of sections 261 to 263 or this section.”
(5)Section 266 (controls: supplementary) is amended as follows.
(6)In subsection (1) (Secretary of State's powers exercisable by making regulations or giving directions) for “(8)” substitute “ (9) ”.
(7)In subsection (3) after “section 263(1)” insert “ (a) or (b) ”.
(8)In subsection (4) after “section 263(1)” insert “ (a) and (b) ”.
(9)After subsection (4) insert—
“(4A)The power under section 263(1)(c) is exercisable only with a view to requiring payments to be made which would be reasonable in all the circumstances, bearing in mind in particular—
(a)the need for medicinal products to be available for the health service on reasonable terms, and
(b)the costs of research and development.”
Commencement Information
I6S. 6 in force at 7.8.2017 by S.I. 2017/809, reg. 2(e)
(1)The National Health Service Act 2006 is amended as follows.
(2)Section 260 (control of maximum price of medical supplies, other than health service medicines) is amended in accordance with subsections (3) and (4).
(3)In subsection (1) for “this Act” substitute “ the health service ”.
(4)After subsection (1) insert—
“(1A)Before making an order under subsection (1) the Secretary of State must consult any body which appears to the Secretary of State appropriate to represent persons who manufacture, distribute or supply medical supplies falling within subsection (1).”
(5)In section 265 (enforcement)—
(a)in subsection (1) for “regulations or directions under sections 261” substitute “ orders, regulations or directions under sections 260 ”,
(b)in subsection (5) for “261” substitute “ 260 ”, and
(c)in subsection (8) for “261” substitute “ 260 ”.
(6)In section 266(6) (interpretation) for “261” substitute “ 260 ”.
(7)In section 272(6) (orders, regulations, rules and directions subject to affirmative procedure), after paragraph (a) insert—
“(aa)the first order under section 260,”.
(8)In section 278(3) (provisions which extend to Scotland and Northern Ireland) for “261” substitute “ 260 ”.
(9)In Schedule 22 (which makes further provision in relation to section 260) omit paragraph 1 (which specifies provision which may be made by an order under section 260).
Commencement Information
I7S. 7 in force at 7.8.2017 by S.I. 2017/809, reg. 2(f)
After section 264 of the National Health Service Act 2006 insert—
(1)References in this section to a UK producer are to a person who manufactures, distributes or supplies any UK health service products.
(2)Regulations may require any UK producer to—
(a)record and keep information which the Secretary of State may require for the purpose specified in subsection (3), and
(b)provide that information to the Secretary of State,
(subject to subsection (9)).
(3)The purpose is that of enabling or facilitating any of the following—
(a)the determination of the payments to be made to any persons who provide primary medical services under Part 4;
(b)the determination of the remuneration to be paid to any persons who provide pharmaceutical services under Part 7;
(c)the consideration by the Secretary of State of whether—
(i)adequate supplies of English health service products are available, and
(ii)the terms on which those products are available represent value for money;
(d)the determination of the payments to be made to any persons who provide primary medical services under Part 4 of the National Health Service (Wales) Act 2006;
(e)the determination of the remuneration to be paid to any persons who provide pharmaceutical services under Part 7 of that Act;
(f)the consideration by the Welsh Ministers of whether—
(i)adequate supplies of Welsh health service products are available, and
(ii)the terms on which those products are available represent value for money;
(g)the determination of the payments to be made to any persons who provide primary medical services under section 2C(1) of the National Health Service (Scotland) Act 1978 (“the 1978 Act”);
(h)the determination of the remuneration to be paid to any persons who provide pharmaceutical care services under section 2CA(1) of the 1978 Act;
(i)the consideration by the Scottish Ministers of whether—
(i)adequate supplies of Scottish health service products are available, and
(ii)the terms on which those products are available represent value for money;
(j)the determination of the remuneration to be paid to any persons who provide primary medical services or pharmaceutical services under Part 2 or 6 of the Health and Personal Social Services (Northern Ireland) Order 1972 (S.I. 1972/1265 (N.I. 14));
(k)the consideration by a Northern Ireland department of whether—
(i)adequate supplies of Northern Ireland health service products are available, and
(ii)the terms on which those products are available represent value for money;
(l)the exercise by the Secretary of State of any powers under sections 260 to 264 and 265;
(m)the operation of a voluntary scheme.
(4)The information which the Secretary of State may require from a UK producer by virtue of this section includes the following—
(a)the price charged or paid by the producer for UK health service products;
(b)the price charged or paid by the producer for delivery or other services in connection with the manufacturing, distribution or supply of UK health service products;
(c)the discounts or rebates or other payments given or received by the producer in connection with the manufacturing, distribution or supply of UK health service products;
(d)the revenue or profits accrued to the producer in connection with the manufacturing, distribution or supply of UK health service products (including, in relation to profits, the costs incurred by the producer in connection with the manufacturing, distribution or supply of the products);
(e)such information about medicinal products, other medical supplies or other related products as is necessary to verify whether they are UK health service products and, if so, which of the following they are—
(i)English health service products;
(ii)Welsh health service products;
(iii)Scottish health service products;
(iv)Northern Ireland health service products.
(5)Regulations under this section must require the Secretary of State to give a UK producer an information notice if information is required in respect of the costs incurred by the producer in connection with the manufacturing, distribution or supply of a particular UK health service product (other than costs which relate to any transaction between the producer and a UK producer for that product).
(6)An information notice is a notice stating—
(a)the period in relation to or for which, or intervals at which, information is required to be provided,
(b)the form and manner in which information is required to be provided,
(c)the time at which or period within which information is required to be provided, and
(d)that a right of appeal is conferred by virtue of section 265(5A).
(7)Regulations under this section may require information which does not fall within subsection (5) to be provided—
(a)in relation to or for a prescribed period or at prescribed intervals,
(b)in a prescribed form and manner, and
(c)at a prescribed time or within a prescribed period.
(8)The provision of information by virtue of this section does not breach—
(a)any obligation of confidence owed by the person providing it, or
(b)any other restriction on the provision of information (however imposed).
(9)Regulations under this section may not do any of the following—
(a)require any person who provides primary medical services under Part 4 of the National Health Service (Wales) Act 2006, or any person who provides pharmaceutical services under Part 7 of that Act, to record, keep or provide information relating to any Welsh health service products which are supplied by the person in providing the services in question;
(b)require any person who provides primary medical services under section 2C(1) of the 1978 Act, or any person who provides pharmaceutical care services under section 2CA(1) of that Act, to record, keep or provide information relating to any Scottish health service products which are supplied by the person in providing the services in question;
(c)require any person who provides primary medical services or pharmaceutical services under Part 2 or 6 of the Health and Personal Social Services (Northern Ireland) Order 1972 (S.I. 1972/1265 (N.I. 14)) to record, keep or provide information relating to Northern Ireland health service products which are supplied by the person in providing the services in question.
(10)“English health service products” means any medicinal products used to any extent for the purposes of the health service continued under section 1(1) and any other medical supplies, or other related products, required for the purposes of that health service.
(11)“Medical supplies” is to be read in accordance with section 260(5).
(12)“Northern Ireland health service products” means any medicinal products used to any extent for the purposes of health care provided by virtue of the Health and Social Care (Reform) Act (Northern Ireland) 2009 and any other medical supplies, or other related products, required for the purposes of health care provided by virtue of that Act.
(13)“Scottish health service products” means any medicinal products used to any extent for the purposes of the health service within the meaning of the 1978 Act and any other medical supplies, or other related products, required for the purposes of that health service.
(14)“UK health service products” means any English health service products, Welsh health service products, Scottish health service products or Northern Ireland health service products.
(15)“Welsh health service products” means any medicinal products used to any extent for the purposes of the health service continued under section 1(1) of the National Health Service (Wales) Act 2006 and any other medical supplies, or other related products, required for the purposes of that health service.
(16)Until the coming into force of the repeal of section 27 of the 1978 Act by schedule 3 to the Smoking, Health and Social Care (Scotland) Act 2005 the references in subsections (3)(h) and (9)(b) to pharmaceutical care services under section 2CA(1) of the 1978 Act are to be read as references to pharmaceutical services under section 27(1) of that Act.
(1)Information provided by virtue of section 264A may be disclosed by the Secretary of State to any of the following persons—
(a)the Board;
(b)any Special Health Authority;
(c)the Health and Social Care Information Centre;
(d)any government department;
(e)the Welsh Ministers;
(f)the Scottish Ministers;
(g)the Common Services Agency for the Scottish Health Service constituted under section 10 of the 1978 Act;
(h)a Northern Ireland department;
(i)the Regional Business Services Organisation established under section 14 of the Health and Social Care (Reform) Act (Northern Ireland) 2009;
(j)any person who provides services to any person falling within any of paragraphs (a) to (i);
(k)any prescribed body appearing to the Secretary of State to represent UK producers;
(l)such of the following as may be prescribed—
(i)an NHS foundation trust;
(ii)any health service body within the meaning of section 9(4) (not falling within any of paragraphs (a) to (k) above).
(2)A person to whom any confidential or commercially sensitive information is disclosed under subsection (1) may not—
(a)use the information for any purpose other than the purpose specified in relation to that person in subsection (3), or
(b)disclose the information to another person (subject to subsection (4)).
(3)For the purposes of subsection (2)—
(a)in relation to a person falling within subsection (1)(a) to (c), the purpose is that of exercising functions connected with any of the matters specified in section 264A(3)(a) to (c), (l) or (m);
(b)in relation to a person falling within subsection (1)(d), the purpose is that of—
(i)exercising functions connected with any of the matters specified in section 264A(3)(a) to (c), (l) or (m), or
(ii)preventing, detecting or investigating any unlawful activities;
(c)in relation to a person falling within subsection (1)(e), the purpose is that of exercising functions connected with any of the matters specified in section 264A(3)(d) to (f), (l) or (m);
(d)in relation to a person falling within subsection (1)(f) or (g), the purpose is that of exercising functions connected with any of the matters specified in section 264A(3)(g) to (i), (l) or (m);
(e)in relation to a person falling within subsection (1)(h) or (i), the purpose is that of exercising functions connected with any of the matters specified in section 264A(3)(j) to (m);
(f)in relation to a person falling within subsection (1)(j), the purpose is that of providing services in connection with any purpose specified in relation to the person for whom the services are provided in any of paragraphs (a) to (e) above;
(g)in relation to a person falling within subsection (1)(k) or (l), the purpose is any prescribed purpose connected with any of the matters specified in section 264A(3).
(4)The Welsh Ministers may disclose any confidential or commercially sensitive information disclosed to them under subsection (1) to any of the following persons—
(a)a Local Health Board or other person appointed under section 88(3)(b) of the National Health Service (Wales) Act 2006 to exercise the functions of a determining authority under Part 7 of that Act;
(b)a National Health Service trust established under section 18 of the National Health Service (Wales) Act 2006;
(c)any person who provides services to the Welsh Ministers or to any person falling within paragraph (a) or (b).
(5)A person to whom any confidential or commercially sensitive information is disclosed under subsection (4) may not—
(a)use the information for any purpose other than the purpose of exercising functions connected with any of the matters specified in section 264A(3)(d) to (f), (l) or (m), or
(b)disclose the information to another person.
(1)Before making regulations under section 264A or 264B the Secretary of State must consult any body which appears to the Secretary of State appropriate to represent UK producers.
(2)Nothing in section 264A or 264B requires information to be provided, or authorises information to be disclosed or used, in contravention of the Data Protection Act 1998.
(3)Nothing in section 264A or 264B affects any duties, obligations or powers to require or authorise information to be provided, disclosed or used which exist apart from that section.”
Commencement Information
I8S. 8 in force at 7.8.2017 by S.I. 2017/809, reg. 2(g)
Prospective
“After section 201 of the National Health Service (Wales) Act 2006 insert—
(1)Regulations may make provision requiring any Part 4 provider or Part 7 provider to—
(a)record and keep information, or information of a description, specified in the regulations, and
(b)provide that information to the Welsh Ministers.
(2)Information, or a description of information, may not be specified in the regulations by virtue of subsection (1) unless the Welsh Ministers consider that the information may be required for the purpose of enabling or facilitating any of the following—
(a)the determination of the payments to be made to any Part 4 providers;
(b)the determination of the remuneration to be paid to any Part 7 providers;
(c)the consideration by the Welsh Ministers of whether—
(i)adequate supplies of health service products are available, and
(ii)the terms on which those products are available represent value for money.
(3)The information which the Welsh Ministers may require from a Part 4 provider or Part 7 provider by virtue of this section includes the following—
(a)the price charged or paid by the provider for health service products;
(b)the price paid by the provider for delivery or other services in connection with health service products;
(c)the discounts or rebates or other payments given or received by the provider in connection with the supply of health service products;
(d)the revenue or profits accrued to the provider in connection with the supply of health service products;
(e)such information about medicinal products, other medical supplies or other related products as is necessary to verify whether or not they are health service products.
(4)Regulations under this section may require information to be provided in such form and manner, and at such time or within such period, as may be prescribed.
(5)Regulations under this section may provide for a person who contravenes any provision of the regulations to be liable to pay a penalty to the Welsh Ministers.
(6)The penalty may be—
(a)a single penalty not exceeding £10,000, or
(b)a daily penalty not exceeding £100 for every day on which the contravention occurs or continues.
(7)If regulations under this section make provision by virtue of subsection (5) they must include provision conferring on Part 4 providers and Part 7 providers a right of appeal against a decision of the Welsh Ministers to impose a penalty.
(8)The provision of information by virtue of this section does not breach—
(a)any obligation of confidence owed by the person providing it, or
(b)any other restriction on the provision of information (however imposed).
(9)The Welsh Ministers may by regulations increase (or further increase) either of the sums mentioned in subsection (6).
(10)In this section—
“health service products” means any medicinal products used to any extent for the purposes of the health service continued under section 1(1) and any other medical supplies, or other related products, required for the purposes of that health service;
“medical supplies” includes surgical, dental and optical materials and equipment (and for this purpose “equipment” includes any machinery, apparatus or appliance, whether fixed or not, and any vehicle);
“medicinal product” has the meaning given by section 130 of the Medicines Act 1968;
“Part 4 provider” means a person who provides primary medical services under Part 4;
“Part 7 provider” means a person who provides pharmaceutical services under Part 7.
(1)Information provided by virtue of section 201A may be disclosed by the Welsh Ministers to any of the following persons—
(a)a Local Health Board or other person appointed under section 88(3)(b) to exercise the functions of a determining authority under Part 7;
(b)an NHS trust established under section 18;
(c)any person who provides services to the Welsh Ministers or to any person falling within paragraph (a) or (b);
(d)any body which appears to the Welsh Ministers appropriate to represent Part 4 providers or Part 7 providers (as defined by section 201A(10)).
(2)A person to whom any confidential or commercially sensitive information is disclosed under subsection (1) may not—
(a)use the information for a purpose other than a purpose specified in section 201A(2), or
(b)disclose the information to another person.
(1)Before making regulations under section 201A the Welsh Ministers must consult any body which appears to the Welsh Ministers appropriate to represent Part 4 providers or Part 7 providers.
(2)Nothing in section 201A or 201B requires information to be provided, or authorises information to be disclosed or used, in contravention of the Data Protection Act 1998.
(3)Nothing in section 201A or 201B affects any duties, obligations or powers to require or authorise information to be provided, disclosed or used which exist apart from that section.”
(1)Omit the following provisions of the National Health Service (Scotland) Act 1978—
(a)section 49 (control of maximum prices for medical supplies other than health service medicines), and
(b)Schedule 10 (additional provisions as to control of maximum prices for medical supplies other than health service medicines).
(2)The National Health Service Act 2006 is amended as follows.
(3)In section 260 (control of maximum price of medical supplies other than health service medicines)—
(a)omit subsections (2) to (4), and
(b)in subsection (5) omit—
(i)“and Schedule 22”, and
(ii)the definition of “undertaking” (and the “and” before it).
(4)In section 261 (powers relating to voluntary schemes) omit subsection (7).
(5)In section 263 (statutory schemes)—
(a)in subsection (2) for “(3)” substitute “ (4) ”, and
(b)omit subsection (3).
(6)In section 264 (statutory schemes: supplementary) omit subsection (2).
(7)Section 265 (enforcement) is amended in accordance with subsections (8) to (14).
(8)In subsection (1) for “264” substitute “ 264A ”.
(9)In subsection (5)—
(a)the words from “conferring” to the end become paragraph (a), and
(b)after paragraph (a) insert “, and
(b)conferring on UK producers a right of appeal against enforcement decisions taken in respect of them in pursuance of section 264A and this section (other than enforcement decisions falling within subsection (5A)).”
(10)After subsection (5) insert—
“(5A)Provision must be made by regulations for conferring on UK producers a right of appeal against enforcement decisions taken in respect of them in pursuance of section 264A and this section if the enforcement decisions relate to information notices given by virtue of section 264A(5).”
(11)In subsection (7)(a) and (d) after “supplier” insert “ , or other person who is a UK producer, ”.
(12)In subsection (8) for “264” substitute “ 264A ”.
(13)For subsection (9) substitute—
“(9)Before making any regulations under this section the Secretary of State must consult the industry body and any other body which appears to the Secretary of State appropriate to represent UK producers.”
(14)After subsection (10) insert—
“(11)In this section “UK producer” is to be read in accordance with section 264A.”
(15)In section 271 (territorial limit of exercise of functions), in subsection (3)(i) omit “and Schedule 22”.
(16)In section 272 (orders, regulations, rules and directions) omit subsection (9).
(17)In section 278 (extent), in subsection (3), after “supplies)” insert “ , and this Part to the extent that it applies to those sections, ”.
(18)In Schedule 22 (provisions in relation to section 260) omit paragraphs 2 to 11.
(19)In section 203(6) of the National Health Service (Wales) Act 2006 (statutory instruments which are subject to affirmative procedure) after “section 25B(3)(c) or” insert “ 201A(9) or ”.
Commencement Information
I9S. 10(1)-(18) in force at 7.8.2017 by S.I. 2017/809, reg. 2(h) (with reg. 3)
(1)Subject as follows, this Act extends to England and Wales, Scotland and Northern Ireland.
(2)Sections 1, 2, 9 and 10(19) extend to England and Wales only.
(3)Section 10(1) extends to Scotland only.
(1)Section 11, this section and section 13 come into force on the day on which this Act is passed.
(2)Sections 2, 9 and 10(19) come into force on such day as the Welsh Ministers may by order appoint.
(3)The remaining provisions of this Act come into force on such day as the Secretary of State may by regulations appoint.
(4)An order or regulations under this section may—
(a)appoint different days, or make different provision, for different purposes or areas, and
(b)make transitional, transitory or saving provision.
(5)An order or regulations under this section is or are to be made by statutory instrument.
This Act may be cited as the Health Service Medical Supplies (Costs) Act 2017.
Y Diweddaraf sydd Ar Gael (diwygiedig):Y fersiwn ddiweddaraf sydd ar gael o’r ddeddfwriaeth yn cynnwys newidiadau a wnaed gan ddeddfwriaeth ddilynol ac wedi eu gweithredu gan ein tîm golygyddol. Gellir gweld y newidiadau nad ydym wedi eu gweithredu i’r testun eto yn yr ardal ‘Newidiadau i Ddeddfwriaeth’.
Gwreiddiol (Fel y’i Deddfwyd neu y’i Gwnaed): Mae'r wreiddiol fersiwn y ddeddfwriaeth fel ag yr oedd pan gafodd ei deddfu neu eu gwneud. Ni wnaed unrhyw newidiadau i’r testun.
Rhychwant ddaearyddol: Indicates the geographical area that this provision applies to. For further information see ‘Frequently Asked Questions’.
Dangos Llinell Amser Newidiadau: See how this legislation has or could change over time. Turning this feature on will show extra navigation options to go to these specific points in time. Return to the latest available version by using the controls above in the What Version box.
Testun a grëwyd gan yr adran o’r llywodraeth oedd yn gyfrifol am destun y Ddeddf i esbonio beth mae’r Ddeddf yn ceisio ei wneud ac i wneud y Ddeddf yn hygyrch i ddarllenwyr nad oes ganddynt gymhwyster cyfreithiol. Cyflwynwyd Nodiadau Esboniadol ym 1999 ac maent yn cyd-fynd â phob Deddf Gyhoeddus ac eithrio Deddfau Adfeddiannu, Cronfa Gyfunol, Cyllid a Chyfnerthiad.
Gallwch wneud defnydd o ddogfennau atodol hanfodol a gwybodaeth ar gyfer yr eitem ddeddfwriaeth o’r tab hwn. Yn ddibynnol ar yr eitem ddeddfwriaeth sydd i’w gweld, gallai hyn gynnwys:
This timeline shows the different points in time where a change occurred. The dates will coincide with the earliest date on which the change (e.g an insertion, a repeal or a substitution) that was applied came into force. The first date in the timeline will usually be the earliest date when the provision came into force. In some cases the first date is 01/02/1991 (or for Northern Ireland legislation 01/01/2006). This date is our basedate. No versions before this date are available. For further information see the Editorial Practice Guide and Glossary under Help.
Defnyddiwch y ddewislen hon i agor dogfennau hanfodol sy’n cyd-fynd â’r ddeddfwriaeth a gwybodaeth am yr eitem hon o ddeddfwriaeth. Gan ddibynnu ar yr eitem o ddeddfwriaeth sy’n cael ei gweld gall hyn gynnwys:
liciwch ‘Gweld Mwy’ neu ddewis ‘Rhagor o Adnoddau’ am wybodaeth ychwanegol gan gynnwys
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