Document reference

2023/0131(COD)  
Authorisation and supervision of medicinal products for human use and governing rules for the European Medicines Agency  
Basic information  

2023/0131(COD)

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

Repealing Regulation 2000/141 1998/0240(COD)
Repealing Regulation 2004/726 2001/0252(COD)
Repealing Regulation 2006/1901 2004/0217(COD)
Amending Regulation 2007/1394 2005/0227(COD)
Amending Regulation 2014/536 2012/0192(COD)

Subject
4.20.01 Medicine, diseases
4.20.04 Pharmaceutical products and industry
4.60.08 Safety of products and services, product liability
8.40.08 Agencies and bodies of the EU

Legislative priorities
Joint Declaration 2023-24

Status

Awaiting Council's 1st reading position

 

Key players  
Key events  
26/04/2023
Legislative proposal published
14/09/2023
Committee referral announced in Parliament, 1st reading
14/09/2023
Referral to associated committees announced in Parliament
19/03/2024
Vote in committee, 1st reading
21/03/2024
Committee report tabled for plenary, 1st reading
10/04/2024
Results of vote in Parliament
10/04/2024
Debate in Parliament
10/04/2024
Decision by Parliament, 1st reading
Technical information  
Procedure reference
2023/0131(COD)
Procedure type
COD - Ordinary legislative procedure (ex-codecision procedure)
Procedure subtype
Legislation
Legislative instrument
Regulation

Repealing Regulation 2000/141 1998/0240(COD)

Repealing Regulation 2004/726 2001/0252(COD)

Repealing Regulation 2006/1901 2004/0217(COD)

Amending Regulation 2007/1394 2005/0227(COD)

Amending Regulation 2014/536 2012/0192(COD)

Legal basis
Treaty on the Functioning of the EU TFEU 114; Rules of Procedure EP 57_o; Treaty on the Functioning of the EU TFEU 168-p4
Other legal basis
Rules of Procedure EP 165
Mandatory consultation of other institutions
Stage reached in procedure
Awaiting Council's 1st reading position
Committee dossier
ENVI/9/11874
Documentation gateway  
Transparency  
Meetings with interest representatives published in line with the Rules of Procedure
  • Rapporteurs, Shadow Rapporteurs and Committee Chairs 
    Shadow rapporteur
    ENVI  
    10/04/2024
    Asociación de Sarcomas Grupo Asistencial
    Shadow rapporteur
    ENVI  
    08/04/2024
    Standing Committee of European Doctors
    Rapporteur
    ENVI  
    08/04/2024
    MEDEV
    Shadow rapporteur
    ENVI  
    11/03/2024
    BEAM Alliance
    Shadow rapporteur
    ENVI  
    07/03/2024
    Acumen Public Affairs
    Shadow rapporteur
    ENVI  
    07/03/2024
    EUROPEAN ORGANISATION FOR RARE DISEASES
    Rapporteur
    ENVI  
    06/03/2024
    Beglian PermRep
    Rapporteur
    ENVI  
    05/03/2024
    European Confederation of Pharmaceutical Entrepreneurs
    Rapporteur
    ENVI  
    05/03/2024
    Eurordis - Rare Disease Europe
    Rapporteur
    ENVI  
    05/03/2024
    European Patients' Forum (EPF)
  • Other Members 
    23/07/2024
    Novo Nordisk A/S
    09/07/2024
    Chambre de Commerce et d’Industrie France Pologne
    28/03/2024
    European Federation of Pharmaceutical Industries and Associations
    GSK
    20/03/2024
    BioMarin UK Limited
    19/03/2024
    European Confederation of Pharmaceutical Entrepreneurs
    13/03/2024
    Assosalute
    29/02/2024
    Bayer AG
    27/02/2024
    European Society of Cardiology
    23/02/2024
    European Federation of Pharmaceutical Industries and Associations
    21/02/2024
    Roche Farma