Search Legislation

The Medicines for Human Use and Medical Devices (Fees and Miscellaneous Amendments) Regulations 2002

 Help about what version

What Version

 Help about advanced features

Advanced Features

Changes over time for: The Medicines for Human Use and Medical Devices (Fees and Miscellaneous Amendments) Regulations 2002 (without Schedules)

 Help about opening options

Changes to legislation:

There are currently no known outstanding effects for the The Medicines for Human Use and Medical Devices (Fees and Miscellaneous Amendments) Regulations 2002. Help about Changes to Legislation

Close

Changes to Legislation

Revised legislation carried on this site may not be fully up to date. At the current time any known changes or effects made by subsequent legislation have been applied to the text of the legislation you are viewing by the editorial team. Please see ‘Frequently Asked Questions’ for details regarding the timescales for which new effects are identified and recorded on this site.

Citation, commencement and interpretationU.K.

1.—(1) These Regulations may be cited as the Medicines for Human Use and Medical Devices (Fees and Miscellaneous Amendments) Regulations 2002 and shall come into force on 1st April 2002.

(2) In these Regulations—

  • “the Devices Regulations” means the Medical Devices (Consultation Requirements) (Fees) Regulations 1995 M1;

  • “the General Fees Regulations” means the Medicines (Products for Human Use—Fees) Regulations 1995 M2;

  • “the Homoeopathic Products Regulations” means the Medicines (Homoeopathic Medicinal Products for Human Use) Regulations 1994 M3; and

  • “the Marketing Authorisations Regulations” means the Medicines for Human Use (Marketing Authorisations Etc.) Regulations 1994 M4.

Marginal Citations

M1S.I. 1995/449; amended by S.I.1998/574, 1999/566, 2000/592 and 2001/795.

M2S.I. 1995/1116; amended by S.I. 1996/683, 1998/574, 1999/566, 2000/592 and 3031, and 2001/795.

M3S.I. 1994/105; amended by S.I. 1994/899, 1995/541, 1996/482, 1998/574, 1999/566, 2000/592 and 2001/795.

M4S.I. 1994/3144; amended by S.I. 1998/3105, 2000/292, 2001/795 and 2002/236.

Amendment of the Homoeopathic Products RegulationsU.K.

2.—(1) In regulation 6 of the Homoeopathic Products Regulations (grant of a certificate), omit paragraph (b).

(2) In regulation 9 of the Homoeopathic Products Regulations M5 (suspension and revocation), omit paragraph (3).

(3) In regulation 14 of the Homoeopathic Products Regulations M6 (fees for variations of certificates)—

(a)in paragraph (1)(a), for “£95” substitute “ £103 ”;

(b)in paragraph (1)(b)(i), for “£95” substitute “ £103 ”;

(c)in paragraph (1)(b)(ii), for “£45” substitute “ £51.50 ”;

(d)in paragraph (2)(a), for “£185” substitute “ £200 ”;

(e)in paragraph (2)(b)(i), for “£185” substitute “ £200 ”;

(f)in paragraph (2)(b)(ii), for “£185” substitute “ £200 ”;

(g)in paragraph (2)(b)(iii), for “£88” substitute “ £100 ”; and

(h)in paragraph (2)(b)(iv), for “£44” substitute “ £50 ”.

(4) In regulation 15(1) of the Homoeopathic Products Regulations M7 (fees payable by holders of certificates), for “£12” substitute “ £13 ”.

(5) In the Table in Schedule 2 to the Homoeopathic Products Regulations M8 (fees for applications for the grant of certificates of registration)—

(a)in column (2) (fees for applications in respect of products prepared from not more than 5 homoeopathic stocks)—

(i)for “£113” substitute “ £122 ”,

(ii)for “£341” substitute “ £368 ”, and

(iii)for “£562” substitute “ £607 ”; and

(b)in column (3) (fees for other applications)—

(i)for “£280” substitute “ £302 ”,

(ii)for “£502” substitute “ £542 ”, and

(iii)for “£736” substitute “ £795 ”.

Marginal Citations

M5As amended by regulation 3 of S.I. 1994/899.

M6As amended by regulation 3(2) of S.I. 2001/795.

M7As amended by regulation 3(3) of S.I. 2001/795.

M8As amended by regulation 3(4) of S.I. 2001/795.

Amendment of the Marketing Authorisations RegulationsU.K.

3.—(1) The Marketing Authorisations Regulations are amended as follows.

(2) In regulation 5 (consideration, and grant or refusal, of an application for, or for renewal or variation of, a United Kingdom marketing authorization), omit paragraph (2).

(3) After regulation 5 (consideration, and grant or refusal, of an application for, or for renewal or variation of, a United Kingdom marketing authorization) insert the following regulation—

Classification of medicinal products

5A.(1) Each marketing authorization granted by the licensing authority on or after 1st April 2002 shall be granted subject to a condition that the medicinal product to which the authorization relates is to be available—

(a)only on prescription;

(b)only from a pharmacy; or

(c)on general sale.

(2) Where prior to 1st April 2002 a medicinal product is subject to a marketing authorization and that authorization contains a statement that it is to be available on one or more of the following bases—

(a)only on prescription;

(b)only from a pharmacy; or

(c)on general sale,

it is a condition of the marketing authorization from 1st April 2002 that the product is to be available only on that basis or, as the case may be, those bases..

(4) In regulation 6 (revocation, suspension or variation of a United Kingdom marketing authorization or the suspension of the use or marketing of medicinal products), omit paragraph (8).

(5) Regulation 8 (control of sale or supply of relevant medicinal products) is hereby revoked.

(6) In paragraph 6(2) of Schedule 5 (labels), for head (a) substitute—

(a)if the product would be subject to restrictions imposed under section 58 of the Act if it contained a higher proportion or level of any substance, except where the product is for external use only or contains any of the substances described in head (c) of this sub-paragraph, the words “Warning. Do not exceed the stated dose”;.

Amendment of regulation 3 of the Devices RegulationsU.K.

4.  In regulation 3 of the Devices Regulations M9 (fees)—

(a)in paragraph (1)(a), for “£3,029” substitute “ £3,271 ”;

(b)in paragraph (1)(b), for “£6,726” substitute “ £7,264 ”;

(c)in paragraph (2)(a), for “£599” substitute “ £647 ”;

(d)in paragraph (2)(b), for “£1,676” substitute “ £1,810 ”;

(e)in paragraph (3)(a), for “£2,285” substitute “ £3,271 ”;

(f)in paragraph (3)(b), for “£6,406” substitute “ £7,264 ”;

(g)in paragraph (4)(a), for “£570” substitute “ £647 ”;

(h)in paragraph (4)(b), for “£1,596” substitute “ £1,810 ”;

(i)in paragraph (5)(a), for “£30,972” substitute “ £33,450 ”; and

(j)in paragraph (5)(b), for “£7,690” substitute “ £8,305 ”.

Marginal Citations

M9As amended by regulation 4 of S.I. 2001/795.

Amendment of the General Fees RegulationsU.K.

F15.  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

Signed by authority of the Secretary of State for Health

Hunt

Parliamentary Under Secretary of State,

Department of Health

Whitty

Parliamentary Under Secretary of State,

Department for Environment, Food and Rural Affairs

Bairbre de Brún

Minister of Health, Social Services and Public Safety

Bríd Rodgers

Minister of Agriculture and Rural Development

We consent,

Anne McGuire

Nick Ainger

Two of the Lords Commissioners of Her Majesty’s Treasury

Back to top

Options/Help

Print Options

Close

Legislation is available in different versions:

Latest Available (revised):The latest available updated version of the legislation incorporating changes made by subsequent legislation and applied by our editorial team. Changes we have not yet applied to the text, can be found in the ‘Changes to Legislation’ area.

Original (As Enacted or Made): The original version of the legislation as it stood when it was enacted or made. No changes have been applied to the text.

Close

See additional information alongside the content

Geographical Extent: Indicates the geographical area that this provision applies to. For further information see ‘Frequently Asked Questions’.

Show Timeline of Changes: 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.

Close

Opening Options

Different options to open legislation in order to view more content on screen at once

Close

More Resources

Access essential accompanying documents and information for this legislation item from this tab. Dependent on the legislation item being viewed this may include:

  • the original print PDF of the as enacted version that was used for the print copy
  • lists of changes made by and/or affecting this legislation item
  • confers power and blanket amendment details
  • all formats of all associated documents
  • correction slips
  • links to related legislation and further information resources
Close

Timeline of Changes

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.

Close

More Resources

Use this menu to access essential accompanying documents and information for this legislation item. Dependent on the legislation item being viewed this may include:

  • the original print PDF of the as made version that was used for the print copy
  • correction slips

Click 'View More' or select 'More Resources' tab for additional information including:

  • lists of changes made by and/or affecting this legislation item
  • confers power and blanket amendment details
  • all formats of all associated documents
  • links to related legislation and further information resources