Document reference

2008/0257(COD)  
Medicinal products for human use: pharmacovigilance of products  
Basic information  

2008/0257(COD)

COD - Ordinary legislative procedure (ex-codecision procedure)
Regulation

Amending Regulation (EC) No 726/2004, Community procedures 2001/0252(COD)
Amending Regulation (EC) No 1394/2007 2005/0227(COD)
See also 2008/0260(COD)

Subject
4.20.04 Pharmaceutical products and industry
4.20.05 Health legislation and policy
4.60.08 Safety of products and services, product liability

Status

Procedure completed

 

Please go to Documentation gateway for any follow-up documents.: Please go to Documentation gateway for any follow-up documents. 
Key players  
Key events  
10/12/2008
Legislative proposal published
COM(2008)0664 Eur-Lex link
13/01/2009
Committee referral announced in Parliament, 1st reading
19/10/2009
Committee referral announced in Parliament, 1st reading
30/11/2009
Debate in Council
2980
27/04/2010
Vote in committee, 1st reading
10/05/2010
Committee report tabled for plenary, 1st reading
A7-0153/2010
21/09/2010
Debate in Parliament
22/09/2010
Results of vote in Parliament
22/09/2010
Decision by Parliament, 1st reading
T7-0331/2010
29/11/2010
Act adopted by Council after Parliament's 1st reading
15/12/2010
Final act signed
15/12/2010
End of procedure in Parliament
31/12/2010
Final act published in Official Journal
Technical information  
Procedure reference
2008/0257(COD)
Procedure type
COD - Ordinary legislative procedure (ex-codecision procedure)
Procedure subtype
Legislation
Legislative instrument
Regulation

Amending Regulation (EC) No 726/2004, Community procedures 2001/0252(COD)

Amending Regulation (EC) No 1394/2007 2005/0227(COD)

See also 2008/0260(COD)

Legal basis
Treaty on the Functioning of the EU TFEU 168-p4; Treaty on the Functioning of the EU TFEU 114-p1
Other legal basis
Rules of Procedure EP 165
Stage reached in procedure
Procedure completed
Committee dossier
ENVI/7/00162
Documentation gateway  
Final act