CHAPTER VI

MODALITIES OF VERIFICATION OF THE SAFETY FEATURES AND DECOMMISSIONING OF THE UNIQUE IDENTIFIER BY PERSONS AUTHORISED OR ENTITLED TO SUPPLY MEDICINAL PRODUCTS TO THE PUBLIC

Obligations of persons authorised or entitled to supply medicinal products to the public
Article 25. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

Derogations from Article 25
Article 26. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

Obligations when applying the derogations
Article 27. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

Obligations when supplying only part of a pack
Article 28. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

Obligations in case of inability to verify the authenticity and decommission the unique identifier
Article 29. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

Actions to be taken by persons authorised or entitled to supply medicinal products to the public in case of suspected falsification
Article 30. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Regulation revoked (31.12.2020) by The Human Medicines (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/775), reg. 1, Sch. 9 para. 1(hh) (subject to transitional provisions in S.I. 2012/1916, Sch. 33A); 2020 c. 1, Sch. 5 para. 1(1)