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The Medicines for Human Use (Fees and Miscellaneous Amendments) Regulations 2003

S.I. 2003/2321 · Made 8 September 2003 · Extends to United Kingdom

Up to date with all changes known to legislation.gov.uk, revised to 1 April 2009.

FEES AND CHARGES

MEDICINES

Made 8th September 2003

Laid before Parliament 9th September 2003

Coming into force

For the purposes of regulations 7(2)(a)(ii) & (b), (3) & (4)(a), 8(2)(b) & (3), 9, 11(2)(a), (b) & (c)(i), (ii), (iii)(aa) & (iv), (3), (4) & (6) and 13 1st October 2003

For all other purposes 31st October 2003

The Secretary of State, being a Minister designated for the purposes of section 2(2) of the European Communities Act 1972 M1 in relation to medicinal products M2, in exercise of the powers conferred upon him by the said section 2(2), the Secretary of State, with the consent of the Treasury, in exercise of the powers conferred upon him by section 56(1) and (2) of the Finance Act 1973 M3, the Secretary of State, the Department of Health, Social Services and Public Safety and the Department of Agriculture and Rural Development, acting jointly and with the consent of the Treasury, in exercise of powers conferred upon them by section 1(1) and (2) of the Medicines Act 1971 M4, or, as the case may be, powers conferred by those provisions and now vested in them M5, and in each case in exercise of all other powers respectively enabling them in that behalf, after consultation in accordance with section 129(6) of the Medicines Act 1968 M6 with such organisations as appear to them to be representative of interests likely to be substantially affected, hereby make the following Regulations:

Annotations to the whole text

Marginal citations

M1

1972 c. 68.

M2

S.I. 1972/1811.

M3

1973 c. 51.

M4

1971 c. 69; as amended by section 21 of the Health and Medicines Act 1988 (c. 49). By virtue of section 1(3) of the 1971 Act, expressions used in that section have the same meaning as in the Medicines Act 1968 (c. 67); see therefore section 1(1) of the 1968 Act, as amended by article 2(2) of, and Schedule 1 to, S.I. 1969/388, by article 5 of, and the Schedule to, S.I. 1999/3142, and by article 5(1) of, and paragraph 15 of Schedule 1 to, S.I. 2002/794, which contains a definition of “the Ministers” which is relevant to the powers being exercised in the making of these Regulations. See also regulation 9(12) of the Medicines for Human Use (Marketing Authorisations Etc.) Regulations 1994 (S.I. 1994/3144), by virtue of which the references in section 1(1) and (2)(b) of the 1971 Act to a licence under Part II of the 1968 Act include reference to a marketing authorization under the 1994 Regulations.

M5

In the case of the Secretary of State, by virtue of article 2(1) of, and paragraph 1 of the Schedule to, S.I. 1999/3142 and article 3(1)(c) and (7) of, and paragraph 15 of Schedule 1 to, S.I. 2002/794; and in the case of the Department of Health, Social Services and Public Safety and the Department of Agriculture and Rural Development, by virtue of the powers vested in the Ministers in charge of those Departments by virtue of section 95(5) of, and paragraph 10 of Schedule 12 to, the Northern Ireland Act 1998 (c. 47) which may now be exercised by the Departments by virtue of section 1(8) of, and paragraph 4(1)(b) of the Schedule to, the Northern Ireland Act 2000 (c. 1); the Departments were renamed by virtue of Article 3(4) and (6) of S.I. 1999/283 (N.I.1).

M6

1968 c. 67; section 129(6) was extended by section 1(3)(b) of the Medicines Act 1971.

Contents

  1. 1Citation, commencement and interpretation
  2. 2Amendment of the Medicines Act 1968
  3. 3Amendment of the Standard Provisions Regulations 1971
  4. 4Amendment of the Product Licences Regulations 1993
  5. 5Amendment of the Homoeopathic Medicinal Products for Human Use Regulations 1994
  6. 6Amendment of the Advertising Regulations 1994
  7. 7Amendment of the Medicines for Human Use (Marketing Authorisations Etc.) Regulations 1994
  8. 8Amendment of regulation 2 of the General Fees Regulations
  9. 9Amendment of regulation 3B of the General Fees Regulations Repealed
  10. 10Amendment of Part II of Schedule 1 to the General Fees Regulations Repealed
  11. 11Amendment of Part III of Schedule 1 to the General Fees Regulations Repealed
  12. 12Amendment of Schedule 3 to the General Fees Regulations Repealed
  13. 13Amendment of Schedule 5 to the General Fees Regulations Repealed
  14. Signature
  15. Explanatory note

1Citation, commencement and interpretation

(1)

These Regulations may be cited as the Medicines for Human Use (Fees and Miscellaneous Amendments) Regulations 2003.

(2)

These Regulations shall come into force—

(a)

for the purposes of—

(i)

regulation 7(2)(a)(ii) and (b), (3) and (4)(a),

(ii)

regulation 8(2)(b) & (3),

(iii)

regulation 9,

(iv)

regulation 11, except paragraphs (2)(c)(iii)(bb) and (5), and

(v)

regulation 13,

on 1st October 2003, and

(b)

for all other purposes, on 31st October 2003.

(3)

In these Regulations, “the General Fees Regulations” means the Medicines (Products for Human Use—Fees) Regulations 1995 M1.

2Amendment of the Medicines Act 1968

In the Medicines Act 1968 M1, in section 132 (interpretation), in paragraph (1), in the definition of “the 2001 Directive”, after “human use”insert “ , as amended M2 ”.

3Amendment of the Standard Provisions Regulations 1971

In the Medicines (Standard Provisions for Licences and Certificates) Regulations 1971 M1—

(a)

in regulation 2 (interpretation), in paragraph (1), in the definition of “the 2001 Directive”, after “human useinsert “ , as amended ”; and

(b)

in Part I of Schedule 1 (standard provisions for product licences), in paragraph 16, for “Part 4G of Annex I to the 2001 Directive” substitute “ point 6 of Part II of Annex I to the 2001 Directive ”.

4Amendment of the Product Licences Regulations 1993

In the Medicines (Applications for Grant of Product Licences—Products for Human Use) Regulations 1993 M1—

(a)

in regulation 1 (citation, commencement and interpretation), in paragraph (2), in the definition of “the 2001 Directive”, after “human use” insert “ , as amended ”; and

(b)

in Schedule 1 (information, documents etc. required in respect of applications)—

(i)

in paragraph 17, for “Part 3, paragraph 1.1, second sub-paragraph of the Annex I to the 2001 Directive” substitute “ paragraph (9) of the Introduction and general principles of Annex I to the 2001 Directive ”, and

(ii)

in paragraph 18, for “Part 4, paragraph B.2 of the Annex I to the 2001 Directive” substitute “ paragraph 5.2(a) of Part I of Annex I to the 2001 Directive ”.

5Amendment of the Homoeopathic Medicinal Products for Human Use Regulations 1994

In the Medicines (Homoeopathic Medicinal Products for Human Use) Regulations 1994 M1, in regulation 1 (citation, commencement and interpretation), in paragraph (2), in the definition of “the 2001 Directive”, after “human use” insert “ , as amended ”.

6Amendment of the Advertising Regulations 1994

In the Medicines (Advertising) Regulations 1994 M1, in regulation 1 (interpretation), in paragraph (1), in the definition of “the 2001 Directive”, after “human use” insert “ , as amended ”.

7Amendment of the Medicines for Human Use (Marketing Authorisations Etc.) Regulations 1994

(1)

The Medicines for Human Use (Marketing Authorisations Etc.) Regulations 1994 M1 shall be amended as follows.

(2)

In regulation 1 (citation, commencement and interpretation)—

(a)

in paragraph (2)—

(i)

in the definition of “the 2001 Directive”, after “human use” insert “ , as amended ”, and

(ii)

in the definition of “the relevant Community provisions”M2—

(aa)

omit “Regulation (EC) No. 541/95, as amended” and “Regulation (EC) No. 542/95, as amended”, and

(bb)

after “Regulation (EC) No. 847/2000” insert the following entries—

“Regulation (EC) No. 1084/2003 M3, and Regulation (EC) No. 1085/2003 M4;”; and

(b)

in paragraph (4), after sub-paragraph (b) insert the following sub-paragraph—

“(bb)

any reference in these Regulations to an application for the variation of a marketing authorization includes a reference to a notification of such a variation, and any reference to an applicant for a variation to a marketing authorization includes a reference to a person submitting such a notification; and”.

(3)

After regulation 6 (revocation, suspension or variation of a United Kingdom marketing authorization or the suspension of the use or marketing of medicinal products), insert the following regulation—

“Urgent safety restrictions

6A
(1)

The licensing authority may, subject to and in accordance with the relevant Community provisions, impose an urgent safety restriction M5 on the holder of a United Kingdom marketing authorization.

(2)

Where the licensing authority imposes an urgent safety restriction in accordance with paragraph (1), the holder of the marketing authorization shall—

(a)

implement the restriction within a period specified by the licensing authority; and

(b)

apply to vary the authorization so as to take account of that safety restriction immediately and in any event not later than 15 days after the restriction was imposed.”.

(4)

In Schedule 3 (offences, penalties etc) M6—

(a)

after paragraph 3 insert the following paragraph—

“

3A

Any person who is the holder of a marketing authorization who fails to implement an urgent safety restriction imposed on him by the licensing authority under regulation 6A or by the European Commission under Commission Regulation (EC) No. 1085/2003 shall be guilty of an offence.”; and

(b)

in paragraph 6, in sub-paragraph (c), for “paragraph D of Part 2 of Annex I to the 2001 Directive” substitute “ paragraphs 3.2(9), 3.2.1.2(c) and 3.2.2.4(c) of Part I of Annex I to the 2001 Directive ”.

8Amendment of regulation 2 of the General Fees Regulations

(1)

Regulation 2 of the General Fees Regulations (interpretation) is amended as follows.

(2)

In paragraph (1)—

(a)

in the definition of “the 2001 Directive”, after “human use” insert “ , as amended ”; and

(b)

in the definition of “variation” for “Article 2.1 of Commission Regulation (EC) No. 541/95” substitute “ Article 3.1 of Commission Regulation (EC) No. 1084/2003 ”.

(3)

After paragraph (2) insert the following paragraph—

“(3)

In these Regulations any reference to an application for the variation of a marketing authorization includes a reference to a notification of such a variation, and any reference to an applicant for a variation to a marketing authorization includes a reference to a person submitting such a notification.”.

9Amendment of regulation 3B of the General Fees RegulationsF1

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

10Amendment of Part II of Schedule 1 to the General Fees RegulationsF1

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

11Amendment of Part III of Schedule 1 to the General Fees RegulationsF1

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

12Amendment of Schedule 3 to the General Fees RegulationsF1

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

13Amendment of Schedule 5 to the General Fees RegulationsF1

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

Signature

Signed by authority of the Secretary of State for Health

Warner

Parliamentary Under Secretary of State,

Department of Health

Sealed with the Official Seal of the Department of Health, Social Services and Public Safety

D.C. Gowdy

Permanent Secretary,

Department of Health, Social Services and Public Safety

Sealed with the Official Seal of the Department of Agriculture and Rural Development

Pat Toal

Permanent Secretary,

Department of Agriculture and Rural Development

We consent,

Nick Ainger

Joan Ryan

Two of the Lords Commissioners of Her Majesty’s Treasury

Explanatory note

(This note is not part of the Regulations)

These regulations make amendments to the Medicines Act 1968, the Medicines for Human Use (Marketing Authorisations Etc.) Regulations 1995 (“the Marketing Authorisations Regulations”), the Medicines (Products for Human Use—Fees) Regulations 1995 (“the General Fees Regulations”) and various other statutory instruments relating to medicinal products.

M1M2M3M4M5M6M7M8M9M10M11The Marketing Authorisations Regulations implemented in part the following provisions of European Community law: Council Directives 65/65/EEC , 75/318/EEC , 75/319/EEC and the Regulations adopted by the Commission under Article 15 of that Directive, 89/342/EEC , 89/343/EEC , 89/381/EEC , 92/26/EEC , 92/27/EEC and 92/73/EEC , now repealed and re-enacted by Directive 2001/83/EC (“the 2001 Directive”), and Council Regulation (EEC) No. 2309/93 and the Regulations adopted by the Commission under Article 15.4 or 22.1 of that Regulation. They provide for the manner of making applications for the grant, renewal or variation of a United Kingdom marketing authorization and for procedures for consideration, revocation, suspension and related matters. Regulation 7 of these Regulations amends the Marketing Authorisations Regulations as a consequence of—

  1. (a)

    M12M13Commission Regulations (EC) No. 1084/2003 and No. 1085/2003 , which make provision in relation to variations of marketing authorizations, including the adoption of urgent safety restrictions by competent authorities, and

  2. (b)

    M14the adoption of Commission Directive 2003/63/EC , which amends the 2001 Directive by substituting a new Annex I setting out standards and protocols in respect of the testing of medicinal products for which applications for marketing authorization are made.

Regulations 2 to 6 amend the Medicines Act and various statutory instruments, so as to amend references to the 2001 Directive as a consequence of the adoption of Commission Directive 2003/63/EC.

The General Fees Regulations make provision for the fees payable under the Medicines Act 1971 relating to marketing authorizations, licences and certificates in respect of medicinal products for human use and for certain other fees arising out of or relating to Community obligations in relation to such products. Regulations 8, 10 to 12 make changes to the provisions for fees for applications for marketing authorizations, and for variations of such authorizations, as a consequence of the adoption of Commission Regulation (EC) No. 1084/2003 and Commission Directive 2003/63/EC. In particular, regulation 11 makes provision for new fees for minor variations of Type IA and Type IB and for variations to add new indications for use of a product in a different therapeutic area or in respect of a different organ or other part of the human body (“Extended Type II Complex Variation Applications”). Regulation 9 amends regulation 3A of the General Fees Regulations so as to make provision for fees in respect of meetings at which the licensing authority provide scientific advice to potential applicants for variations to marketing authorizations. Regulation 13 amends Schedule 5 of the General Fees Regulations, which relates to refunds and waivers. Regulation 13(2) makes provision for the waiver of fees payable in connection with meetings at which the licensing authority provide scientific advice to potential applicants for marketing authorizations or variations of such authorizations. Regulation 13(3) provides for the waiver of fees for applications for variations of marketing authorizations which result from urgent safety restrictions imposed by the licensing authority.

A Regulatory Impact Assessment in relation to these Regulations has been placed in the libraries of both Houses of Parliament, and copies can be obtained from the Medicines and Healthcare products Regulatory Agency, Room 16-107, Market Towers, 1 Nine Elms Lane, London SW8 5NQ.