1995/0013(COD)

In vitro diagnostic medical devices: security requirements

Basic information

1995/0013(COD)

COD - Ordinary legislative procedure (ex-codecision procedure)

Directive

Repealed by 2012/0267(COD)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

Date Event Reference Summary
24/10/1994 Additional information
19/04/1995 Legislative proposal published COM(1995)0130
15/05/1995 Committee referral announced in Parliament, 1st reading
06/02/1996 Vote in committee, 1st reading
06/02/1996 Committee report tabled for plenary, 1st reading A4-0031/1996
12/03/1996 Decision by Parliament, 1st reading T4-0115/1996
12/03/1996 Debate in Parliament
20/12/1996 Modified legislative proposal published COM(1996)0643
21/05/1997 Debate in Council
23/03/1998 Council position published 05255/1/1998
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 A4-0225/1998
17/06/1998 Debate in Parliament
18/06/1998 Decision by Parliament, 1st 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
Repealed by 2012/0267(COD)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

Additional information

Source Document Date
European Commission EUR-Lex