Compulsory Licensing of Pharmaceutical Patents for Export Regulation
Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL on compulsory licensing of patents relating to the manufacture of pharmaceutical products for export to countries with public health problems
- Stage
- In force, reached 9 Jun 2006
- In force
- In force since 29 Jun 2006 · CELEX 32006R0816
- Procedure
- Regulation · Ordinary legislative procedure
- Last activity
- 29 Jun 2006
Where it stands
Latest: Publication in the Official Journal, 9 Jun 2006.
- 1 Dec 2005
- EP position at first reading
- 17 May 2006
- Signature by the president of the EP and by the president of the Council
- 9 Jun 2006
- Publication in the Official Journal
Documents
Newest first. Each opens at its source.
- Text adopted · OJ L 157 09.06.2006, p. 0001-0007Commission · 9 Jun 2006
- Text adopted · Regulation 2006/0816Commission · 17 May 2006
- OJ C 286 17.11.2005, p. 0004-0007Commission · 17 Nov 2005
- Report · A6-0242/2005Parliament
- Committee opinion · PE353.621Parliament
- Committee opinion · PE355.333Parliament
- Committee opinion · PE357.740Parliament
- Amendments · PE360.027Parliament
- SEC(2004)1348Commission
- Text adopted · SP(2005)5015Parliament
- Text adopted · T6-0454/2005Parliament
Summary
GeneratedRegulation (EC) No 816/2006 sets a harmonized EU procedure for granting compulsory licenses on pharmaceutical patents and supplementary protection certificates for manufacture and export to eligible importing countries. It entered into force on the 20th day after its 9 June 2006 publication.
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Sources: EP Legislative Observatory · EU Law Tracker · EUR-Lex. Record as of 12 Oct 2026. Something wrong on this page? Report an error.
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