Document reference

1997/0197(COD)  
Medicinal products for human use: implementation of good clinical practice in the conduct of clinical trials  
Basic information  

1997/0197(COD)

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

Amended by 2004/0217(COD)
Repealed by 2012/0192(COD)
Amended by 2021/0431(COD)

Subject
4.20.02.06 Clinical practice and experiments
4.20.04 Pharmaceutical products and industry

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  
03/09/1997
Legislative proposal published
COM(1997)0369 Eur-Lex link
19/09/1997
Committee referral announced in Parliament, 1st reading
29/10/1998
Vote in committee, 1st reading
29/10/1998
Committee report tabled for plenary, 1st reading
A4-0407/1998
16/11/1998
Debate in Parliament
17/11/1998
Decision by Parliament, 1st reading
T4-0648/1998
26/04/1999
Modified legislative proposal published
COM(1999)0193 Eur-Lex link
20/07/2000
Council position published
08878/1/2000
07/09/2000
Committee referral announced in Parliament, 2nd reading
21/11/2000
Vote in committee, 2nd reading
21/11/2000
Committee recommendation tabled for plenary, 2nd reading
A5-0349/2000
11/12/2000
Debate in Parliament
12/12/2000
Decision by Parliament, 2nd reading
T5-0548/2000
26/02/2001
Act approved by Council, 2nd reading
04/04/2001
Final act signed
04/04/2001
End of procedure in Parliament
01/05/2001
Final act published in Official Journal
Technical information  
Procedure reference
1997/0197(COD)
Procedure type
COD - Ordinary legislative procedure (ex-codecision procedure)
Procedure subtype
Legislation
Legislative instrument
Regulation

Amended by 2004/0217(COD)

Repealed by 2012/0192(COD)

Amended by 2021/0431(COD)

Legal basis
EC Treaty (after Amsterdam) EC 095
Stage reached in procedure
Procedure completed
Committee dossier
ENVI/5/13000
Documentation gateway  
Final act