The pharmaceutical analysis laboratory offers its services to manufacturers, importers and exporters of human and veterinary medicinal products, healthcare facilities, research and development facilities in the pharmaceutical industry, state administration bodies and public entities.
The pharmaceutical analysis laboratory holds the Certificate of Good Manufacturing Practice (GMP) issued by SÚKL for the testing of human medicines and the authorisation of ISCVBL for the testing of veterinary medicines. Furthermore, it is regularly audited by our Czech and foreign customers and their respective supervisory bodies - SÚKL, FDA.
The pharmaceutical analysis laboratory offers services in the following areas:
- Quality control of final products (human and veterinary medicines) for batch release to the market
- Testing of raw materials and intermediate products in drug manufacturing
- Development, validation and verification of analytical methods
- Analyses according to ČL, Ph.Eur., USP