Retained EU Law
2009
United Kingdom
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)
At a glance
What this Act requires
Sections that create concrete duties on businesses or carry penalties. Procedural and definitional sections are folded into the “Browse other sections” expander at the bottom of each group. Click any section title to read the source text on legislation.gov.uk.
Browse 28 other sections — procedural / definitional / commencement
Definitions
Scope
Conditions for obtaining a certificate
Subject matter of protection
Effects of the certificate
Entitlement to the certificate
Application for a certificate
Content of the application for a certificate
Lodging of an application for a certificate
Grant of the certificate or rejection of the application for a certificate
Publication
Fees
Duration of the certificate
Authorisation granted after submission of an application for a certificate
Extension of the duration of a certificate
Expiry of the certificate
Invalidity of the certificate
Revocation of an extension of the duration
Notification of lapse or invalidity
Appeals
Procedure
Transitional provisions
Additional provisions relating to the enlargement of the Community
Transitional provisions
Evaluation
Repeal
Entry into force
Explore more
Browse legislation
Find other UK business legislation with related guidance.