Brussels, 27.4.2023

COM(2023) 231 final

ANNEXES

to the

Proposal for a Regulation of the European Parliament and of the Council

on the supplementary protection certificate for medicinal products (recast)

{SEC(2023) 172 final} - {SWD(2023) 117 final} - {SWD(2023) 118 final} - {SWD(2023) 119 final}


🡻 469/2009 (adapted)

ANNEX I

Repealed Regulation with list of its successive amendments ⌦ the amendment thereto ⌫

·Council Regulation (EEC) No 1768/92

·( OJ L 182, 2.7.1992, p. 1 )

· 

·Annex I, point XI.F.I, of the 1994 Act of Accession

·( OJ C 241, 29.8.1994, p. 233 )

· 

·Annex II, point 4.C.II, of the 2003 Act of Accession

·( OJ L 236, 23.9.2003, p. 342 )

· 

·Annex III, point 1.II, of the 2005 Act of Accession

·( OJ L 157, 21.6.2005, p. 56 )

· 

·Regulation (EC) No 1901/2006 of the European Parliament and of the Council

·( OJ L 378, 27.12.2006, p. 1 )

·Only Article 52

⌦ Regulation (EC) No 469/2009 of the European Parliament and of the Council

(OJ L 152, 16.6.2009, p. 1) ⌫

⌦ Regulation (EU) 2019/933 of the European Parliament and of the Council

(OJ L 153, 11.6.2019, p. 1) ⌫

⌦ 2012 Act of Accession 

(OJ L112, 24.2.2012, p. 21) ⌫

⌦ Only Annex III, point 1(2)(II)(2) ⌫



🡻 2019/933 Art. 1 pt. 6

ANNEX II-I

Logo

This logo shall appear in black and in such a size as to be sufficiently visible.

’