The State Agency of Medicines:
Management Board of the European Medicines Agency (EMA), EMA Committees and Working Parties
| Committee for Medicinal Products for Human Use | CHMP |
| CHMP Quality Working Party | CHMP Quality Working Party |
| CHMP Safety Working Party | CHMP Safety Working Party |
| CHMP Biologics Working Party | CHMP Biologics Working Party |
| CHMP Blood Products Working Party | CHMP Blood Products Working Party |
| CHMP Working Group on Quality Review of Documents | CHMP Working Group on Quality Review of Documents |
| Active Substance Master File Working Group | ASMF |
| Pharmacovigilance Risk Assessment Committee | PRAC |
| Paediatric Committee | PDCO |
| Committee for Orphan Medicinal Products | Committee for Orphan Medicinal Products |
| Committee on Herbal Medicinal Products | HMPC |
| Committee for Advanced Therapies | CAT |
| GCP Inspectors Working Group | GCP Inspectors Working Group |
| EudraVigilance Telematics Implementation Group | EudraVigilance Telematics Implementation Group |
| IT Directors Group | IT Directors Group |
| Meetings of Good Manufacturing Practice inspectors | GMDP Inspectors Working Group |
| Meetings of Pharmacovigilance inspectors | PhV Inspectors Working Group |
| CHMP Oncology Working Group | CHMP Oncology Working Group |
The Heads of Medicines Agencies' (HMA) Working Groups
| Homeopathic Medicinal Products Working Group | HMPWG |
| Coordination Group for Mutual Recognition and Decentralized Procedures - Human | CMD (H) |
| Clinical Trials Facilitation Group | CTFG |
| HMA Working Group of Quality Managers | WGQM |
| HMA Pharmacovigilance Audit Facilitation Group | PAFG |
| Working Group of Communication Professionals | WGCP |
Competent Authorities for Medical Devices in the European Union
Contents will be added.
European Commission Committees and Working Groups
| Standing Committee | Standing Committee |
| Pharmaceutical Committee | |
| Notice to Applicants Working Group | Notice to Applicants |
| Ad hoc group for development of implementing guidelines for Directive 2001/20/EC | Implementing guidelines for Directive 2001/20/EC ad hoc group |
| Drug Precursors Working Group | Drug Precursors Working Group |
| European Medicines Agencies Cooperation on Legal Issues | EMACOLEX |
| Competent authorities for human blood, tissues and cells, organs | |
| Medical Device Expert Group | MDEG - Medical Device Expert Group |
| Working Group on Clinical Investigation and Evaluation of medical devices | WG on Clinical Investigation and Evaluation |
| Medical Devices Vigilance Experts Group | MD Vigilance Experts Group |
| Medical Devices Committee | Medical Devices Committee |
The European Council
| Proficiency Testing Scheme (PTS) organised by the European Directorate for the Quality of Medicines (EDQM) | PTS |
| Annual meetings of the EC Official Medicines Control Laboratory (OMCL) | OMCL Annual Meeting |
| EDQM European Pharmacopoeia Commission | |
| European Directorate for the Quality of Medicines dedicated to Centrally Authorised Products (CAP) | CAP Annual Meeting |
| EDQM certification of suitability to monographs of the European Pharmacopoeia | CEP |
| Testing programme for medicinal products authorised in the Mutual Recognition Procedure and Decentralized Procedure (MRP/DCP) coordinated by the European Directorate for the Quality of Medicines | MRP/DCP Testing Programme |
| Testing programme for Centrally Authorised Products | CAP Testing Programme |
| European Market Surveillance Study (MSS) coordinated by the European Directorate for the Quality of Medicines | Market Surveillance Study (MSS) |
| Council's Working Party on Pharmaceuticals and Medical Devices | Council’s Working Party on Pharmaceuticals and Medical Devices |
| European Directorate for the Quality of Medicines' Committee on Pharmaceuticals and Pharmaceutical Care |
Medicines agencies in Estonia and Lithuania
Contents will be added.
European Economic Area countries in the field of adverse drug reaction information
Contents will be added.
Meetings of the Heads of the Competent Authorities for Medical Devices
Contents will be added.
Management Committee (CMC - working group of experts from competent authorities for medical devices)
Contents will be added.
Pharmaceutical Inspection Cooperation Scheme (PIC/S) Committee.
Contents will be added.
Interlaboratory proficiency testing organized by the International Pharmaceutical Federation
Contents will be added.
Memorandum of Agreement with the State Food and Drug Administration of the People's Republic of China on cooperation in the normative regulation of medicinal products
Contents will be added.
