Document reference

1995/0013(COD)  
In vitro diagnostic medical devices: security requirements  
Basic information  

1995/0013(COD)

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

Amending  Directive 93/42/EEC 
Amending  Directive 89/392/EEC 
Repealed by 2012/0267(COD)

Subject
2.10.03 Standardisation, EC/EU standards and trade mark, certification, compliance
4.20.02 Medical research
4.20.04 Pharmaceutical products and industry
4.60.02 Consumer information, advertising, labelling

Status

Procedure completed

 

Key players  
Key events  
24/10/1994
Additional information
19/04/1995
Legislative proposal published
COM(1995)0130 Eur-Lex link
15/05/1995
Committee referral announced in Parliament, 1st reading/single reading
06/02/1996
Vote in committee, 1st reading/single reading
06/02/1996
Committee report tabled for plenary, 1st reading/single reading
12/03/1996
Debate in Parliament
12/03/1996
Decision by Parliament, 1st reading/single reading
T4-0115/1996
20/12/1996
Modified legislative proposal published
COM(1996)0643 Eur-Lex link
21/05/1997
Debate in Council
23/03/1998
Council position published
02/04/1998
Committee referral announced in Parliament, 2nd reading
03/06/1998
Vote in committee, 2nd reading
03/06/1998
Committee recommendation tabled for plenary, 2nd reading
17/06/1998
Debate in Parliament
18/06/1998
Decision by Parliament, 2nd reading
T4-0362/1998
05/10/1998
Act approved by Council, 2nd reading
27/10/1998
Final act signed
27/10/1998
End of procedure in Parliament
07/12/1998
Final act published in Official Journal
Technical information  
Procedure reference
1995/0013(COD)
Procedure type
COD - Ordinary legislative procedure (ex-codecision procedure)
Procedure subtype
Legislation
Legislative instrument
Directive

Amending  Directive 93/42/EEC 

Amending  Directive 89/392/EEC 

Repealed by 2012/0267(COD)

Legal basis
EC before Amsterdam E 100A
Stage reached in procedure
Procedure completed
Committee dossier
ECON/4/09931
Documentation gateway  
Final act