The Medicines (Data Sheet) Amendment Regulations 1996

• Citation: S.I. 1996/2420
• Sections: 8

Section 1 Citation, commencement and interpretation

(1) These Regulations may be cited as the Medicines (Data Sheet) Amendment Regulations 1996 and subject to paragraph (2) of this regulation shall come into force on 10th October 1996.

(2) Regulation 4 shall come into force immediately after regulation 3(b).

(3) In these Regulations, “the principal Regulations ” means the Medicines (Data Sheet) Regulations 1972 .

Section 2 Amendment of regulation 1 of the principal Regulations

Regulation 1 of the principal Regulations shall be amended so that—

(a) in paragraph (2) after the definition of “monograph” the following definitions are inserted—

“product information compendium” has the meaning it bears in regulation 2A(1)(b);

“summary of product characteristics” has the meaning it bears in regulation 2(1) of the Medicines (Advertising) Regulations 1994 ;

(b) after paragraph (2) the following paragraph is inserted—

(2A) In these Regulations unless the context otherwise requires “product licence” includes a marketing authorisation in respect of medicinal products intended for use by being administered to human beings and granted under Council Regulation ( EEC ) No. 2309/93 or under the Medicines for Human Use (Marketing Authorisations, Etc.) Regulations 1994 ;

Section 3 Amendment of regulation 2 of the principal Regulations

Regulation 2 of the principal Regulations (form of data sheets) shall be amended so that—

(a) in paragraph (1) after the words “for the purposes of the Act , every data sheet” the words “in respect of medicinal products for use by being administered to animals” are inserted, and

(b) in paragraphs (2) and (3) for the words “regulations 3 and 4” there are substituted the words “regulation 4”.

Section 4 Insertion of regulation 2A in the principal Regulations

After regulation 2 of the principal Regulations there shall be inserted the following regulation—

Data Sheets for medicinal products for human use

(2A)

(1) Subject to the following provisions of these Regulations, for the purposes of the Act every data sheet in respect of medicinal products for use by being administered to human beings shall be either in the form of—

(a) a loose sheet containing the particulars specified in these Regulations, or

(b) a page or part of a page, containing such particulars and forming part of a publication (in these Regulations referred to as a “product information compendium”) consisting of a list of entries in respect of such medicinal products (whether or not it also consists of summaries of product characteristics, or other explanatory material which may be of use to the practitioner).

(2) The provisions of paragraphs (2) and (5) of regulation 2 shall apply in respect of data sheets to which paragraph (1) of this regulation applies as they apply in respect of data sheets to which regulation 2 applies but as if in paragraph (2) for the words “regulation 4” there were substituted “regulation 3”.

Section 5 Amendment of regulation 3 of the principal Regulations

In regulation 3(8) and (9) of the principal Regulations (particulars in data sheets relating to medicinal products for human use) for the words “data sheet compendium” wherever they appear there shall be substituted the words “product information compendium”.

Section 6 Amendment of Schedule 1 to the principal Regulations

Schedule 1 to the principal Regulations shall be amended so that—

(a) at the beginning for the reference to “Regulation 2(2) and 3” a reference to “Regulations 2(2) and (3) and 2A(2)” is substituted, and

(b) at the end of the heading of Part II after the word “REQUIREMENTS” the words “IN RESPECT OF MEDICINAL PRODUCTS FOR USE BY BEING ADMINISTERED TO ANIMALS” are added.

Section 7 Amendment of Schedule 2 to the principal Regulations

In paragraph 10 of column 2 (particulars) of Schedule 2 (particulars required in data sheets relating to medicinal products for human use) for the words “data sheet compendium” there shall be substituted the words “product information compendium”.

Section 8 Revocation

Regulation 6 (temporary provisions) of the principal Regulations shall be revoked.