1993 No. 832
MEDICINES

The Medicines (Applications for Manufacturer’s and Wholesale Dealer’s Licences) Amendment Regulations 1993

Made
Laid before Parliament
Coming into force
The Secretary of State concerned with health in England, the Secretaries of State respectively concerned with health and with agriculture in Wales and in Scotland, the Minister of Agriculture, Fisheries and Food, the Department of Health and Social Services for Northern Ireland and the Department of Agriculture for Northern Ireland, acting jointly, in exercise of powers conferred upon them by sections 18 and 129(1) of the Medicines Act 19681 or, as the case may be, those conferred by the said provisions and now vested in them2 and of all other powers enabling them in that behalf, after consulting such organisations as appear to them to be representative of interests likely to be substantially affected by these Regulations3, hereby make the following Regulations:

Citation, commencement and interpretation1.

(1)

These Regulations may be cited as the Medicines (Applications for Manufacturer’s and Wholesale Dealer’s Licences) Amendment Regulations 1993, and shall come into force on 14th April 1993.

(2)

In these Regulations, “the principal Regulations” means the Medicines (Applications for Manufacturer’s and Wholesale Dealer’s Licences) Regulations 19714.

Amendment of regulation 2 of the principal Regulations2.

In paragraph (1) of regulation 2 of the principal Regulations (interpretation), after the definition of “imported ready-made veterinary drug” there shall be inserted the following—

  • ““member” in the expression “member State” means a member of the European Economic Community;”

““product to which Chapters II to V of the 1965 Directive apply” means a medicinal product to which, in accordance with Article 2 of Council Directive 65/65/EEC as amended5, Article 34 of Council Directive 75/319/EEC6, Article 1 of Council Directive 89/342/EEC7, Article 1 of Council Directive 89/343/EEC8 and Article 1 of Council Directive 89/381/EEC9, Chapters II to V of Council Directive 65/65/EEC apply;”.

Amendment of Schedule 2 to the principal Regulations3.

Schedule 2 to the principal Regulations (particulars required on an application for the grant of a wholesale dealer’s licence) shall be amended by inserting after paragraph 8 the following paragraphs—

“8A.

Where the licence is to relate to products to which Chapters II to V of the 1965 Directive apply, the name and address and degrees, diplomas or qualifications of a responsible person who is to carry out the functions specified in paragraph 7A(2) of Schedule 3 to the Medicines (Standard Provisions for Licences and Certificates) Regulations 197110 (in this and the following paragraph referred to as “the Standard Provisions Regulations”).

8B.

Where the licence is to relate to products to which Chapters II to V of the 1965 Directive apply, details of an emergency plan which satisfies the requirements of paragraph 4A of Schedule 3 to the Standard Provisions Regulations.

8C.

Where the licence is to relate to products to which Chapters II to V of the 1965 Directive apply, a statement of any arrangements for keeping records, either in the form of invoices or on computer or in any other form, relating to all products received or dispatched.”.

Signed by authority of the Secretary of State for Health

Brian Mawhinney
Minister of State,
Department of Health
David Hunt
Secretary of State for Wales
Fraser of Carmyllie
Minister of State, Scottish Office

In Witness whereof the Official Seal of the Minister of Agriculture, Fisheries and Food is hereunto affixed

John Selwyn Gummer
Minister of Agriculture, Fisheries and Food

Sealed with the Official Seal of the Department of Health and Social Services for Northern Ireland on

F. A. Elliott
Permanent Secretary

Sealed with the Official Seal of the Department of Agriculture for Northern Ireland on

W. J. Hodges
Permanent Secretary
(This note is not part of the Regulations)

These Regulations further amend the Medicines (Applications for Manufacturer’s and Wholesale Dealer’s Licences) Regulations 1971 (“the 1971 Regulations”) so implementing in part Council Directive 92/25/EEC (OJ No. L113, 30.4.92, p. 1) (“the Directive”) which concerns the wholesale distribution of medicinal products for human use which are marketed within the European Community.

The Regulations insert a new requirement into the 1971 Regulations requiring applicants for wholesale dealer’s licences which relate to products to which Chapters II to V of the 1965 Directive apply (a definition of which is inserted by regulation 2) to give the name and address of a responsible person who is to oversee wholesaling operations. (regulation 3, article 5(b) of the Directive).

Such applicants are also required by the amendments made by these Regulations to submit details of an emergency plan to be instituted where products are recalled (article 6(d) of the Directive) and of arrangements for keeping records relating to products received or dispatched (article 6(e) of the Directive).