# Regulation (EC) No 469/2009 of the European Parliament and of the Council of 6 May 2009 concerning the supplementary protection certificate for medicinal products (Codified version) (Text with EEA relevance), Division 3: Notification of authorisations


For the purposes of Article 13A, the applicant or the certificate holder—
(a)shall notify the comptroller of the grant of a NI authorisation granted before 1 January 2025 in accordance with paragraphs 2 and 3 of Article 13A notwithstanding that it becomes a former NI authorisation on and after 1 January 2025;
(b)shall not be required to notify the comptroller where before the certificate takes effect a GB authorisation becomes a transitioned-UK authorisation.

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Source: https://www.legislation.gov.uk/eur/2009/469/annex/III/division/3. (the official version)
Page: https://openlegislation.uk/eu-regulation-2009-469/annex-III/division-3.
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.