Paragraph 7 InterpretationF1

In this Act—

(a)

“the Medicinal Products Regulation” means F2Regulation (EC) No 469/2009 of the European Parliament and of the Council of 6th May 2009 concerning the supplementary protection certificate for medicinal products, and

(b)

“the Plant Protection Products Regulation” means Regulation (EC) No 1610/96 of the European Parliament and of the Council of 23 July 1996 concerning the creation of a supplementary protection certificate for plant protection products.

Annotations

Textual amendments

F1: Sch. 4A inserted (17.12.2007) by The Patents (Compulsory Licensing and Supplementary Protection Certificates) Regulations 2007 (S.I. 2007/3293), regs. 1(2), 2(3)
F2: Words in Sch. 4A para. 7(a) substituted (1.10.2014) by The Patents (Supplementary Protection Certificates) Regulations 2014 (S.I. 2014/2411), regs. 1(2), 2(3)(a)