Regulation 5 Section 24 of the Act — duration and renewal of licence

In section 24^f1 (duration and renewal of licence)—

(a)

in subsection (1A) after “obligation” there is inserted “(other than an obligation under the 1992 Directive)”;

(b)

in subsection (3)(c) after “this Act” there is inserted “and any Community obligation under the 1965 Directive or the 1992 Directive”; and

(c)

after subsection (6) there is inserted—

“(7)

In this section “the 1992 Directive” means Council Directive 92/27/EEC^f2 of 31st March 1992 on the labelling of medicinal products for human use and on package leaflets.”.

Annotations

Footnotes

f1: Section 24 was amended by regulation 4(4) of S.I. 1977/1050 and regulation 5(4) of (N.I.) S.R. 1977 No. 150, and applied by regulation 2 of, and the Schedule to, the Medicines Act 1968 (Application to Radiopharmaceutical-associated Products) Regulations 1992 See also the Medicines Act (Application to Radiopharmaceutical-associated Products) Regulations 1992 (S.I. 1992/605).
f2: OJ No. L113,30.4.92, p.8.