EDQM FAQs
- General information on Control of Medicines
- Proficiency Testing Scheme (PTS)
- Official Control Authority Batch Release (OCABR) – for human blood-derived medicinal products and vaccines for human use
- Where can I find the list of the Official Medicines Control Laboratories (OMCLs) in the EU/EEA currently involved in Official Control Authority Batch Release (OCABR) for human biological medicinal products?
- Where can I find a list of the Official Medicines Control Laboratories (OMCL) in the EU/EEA with testing competencies for Official Control Authority Batch Release (OCABR) for human biological medicinal products?
- My question about OCABR is not in the FAQs – how can I contact the EDQM?
- Official Control Authority Batch Release (OCABR) and Official Batch Protocol Review (OBPR) – for immunological veterinary medicinal products (IVMPs)
- Where can I find a list of the Official Medicines Control Laboratories (OMCL) in the EU/EEA with testing competencies for official control authority batch release (OCABR) for IVMPs on the restricted list?
- Where can I find the list of the CAs/OMCLs involved in the EU/EEA Veterinary Batch Release Network (VBRN) for Official Control Authority Batch Release (OCABR) and Official Batch Protocol Review (OBPR)?
- Where can I find the restricted list of IVMPs eligible for OCABR in the EU?
- My question about OCABR/OBPR of IVMPs is not in the FAQs – how can I contact the EDQM?
- MRP/DCP Post-marketing surveillance
- Centrally-Authorised Products (CAP) Sampling and Testing Programme
- Gene Therapy