Retained EU Law SI 2009/469 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)

Status
In Force

What it defines

Regulations creating concrete business duties or carrying penalties, grouped as the instrument is structured. Titles link to the source text — blue means you’re leaving for legislation.gov.uk.

28 other provisions — procedural and definitional
s.annex ia para.1 Standard form for notification pursuant to points (b) and (c)...
s.art001 Definitions
s.art002 Scope
s.art003 Conditions for obtaining a certificate
s.art004 Subject matter of protection
s.art005 Effects of the certificate
s.art006 Entitlement to the certificate
s.art007 Application for a certificate
s.art008 Content of the application for a certificate
s.art009 Lodging of an application for a certificate
s.art010 Grant of the certificate or rejection of the application for a certificate
s.art011 Publication
s.art012 Fees
s.art013 Duration of the certificate
s.art013 Authorisation granted after submission of an application for a certificate
s.art013 Extension of the duration of a certificate
s.art014 Expiry of the certificate
s.art015 Invalidity of the certificate
s.art016 Revocation of an extension of the duration
s.art017 Notification of lapse or invalidity
s.art018 Appeals
s.art019 Procedure
s.art019 Transitional provisions
s.art020 Additional provisions relating to the enlargement of the Community
s.art021 Transitional provisions
s.art021 Evaluation
s.art022 Repeal
s.art023 Entry into force

Duty extraction and severity labels are Guvnor’s analysis of the instrument, not the instrument itself. Always verify against the linked source text.