Is your pharmaceutical process compliant to international regulations?
When obtaining Market Authorisation Application (MAA) it is obligatory that the entire production process and product compounds are tested on compliancy to the relevant Pharmacopoeia. Eurofins BioPharma Product Testing Netherlands has various GMP certified laboratories that provide testing solutions to make sure your pharmaceutical product meets all the regulations of:
- United States Pharmacopeia (USP)
- European Pharmacopoeia (EP)
- British Pharmacopoeia (BP)
- Japanese Pharmacopoeia (JP)
Eurofins offers relevant testing solutions
Eurofins BioPharma Product Testing Netherlands provides standard tests or customised packages for testing compliant to all Pharmacopoeia. Read more on our specific testing solutions or contact us if you have any specific requirements:
Why choose Eurofins BioPharma Product Testing Netherlands?
- Single point of contact. Benefit from streamlined communication through a single local point of contact while leveraging the advantages of our extensive global network.
- Complete service portfolio. Leveraging our network of GMP product testing laboratories, we can offer a comprehensive testing service portfolio to our customers.
- Standard and custom solutions. If our standard methods do not meet your needs, our skilled technicians can develop customised testing methods tailored to your specific requirements.
Feel free to contact us to discuss your specific requirements.
