We can perform audits of the entire pharmaceutical supply chain (suppliers, contract manufacturers, etc.) on the basis of international or customer requirements on the following quality systems:
GMP (Good Manufacturing Practice):
- Finished products, APIs and excipients, raw materials,
- Medical devices
- Dietary supplements
- Packaging materials
- Audit of service providers:
- Analytical tests
- Sterilization,
- Maintenance,
- Validation, etc.
GCP (Good Clinical Practice):
- Clinical Research Organization (CRO),
- Test site
- Center, data center.
GLP (Good Laboratory Practice):
- All laboratories used to perform non-clinical safety studies that are intended to support research authorizations or marketing authorizations
GDP (Good Distribution Practice):
- Distribution centers, transport.
It is possible to purchase existing ready-made audit documentation on shared pharmaceutical audits:
Search the database here: https://ha.eurofins-aol.com/audits
Contact:
Dr. Tolokán Antal
+3618723634
tolokan.antal@laboratorium.hu
