Quality control is essential for ensuring that drug products are marketed safely and effectively. From drug development and manufacturing through finished product, Eurofins BioPharma Product Testing routinely performs QC analysis according to cGMP quality standards for Active Pharmaceutical Ingredients (APIs), intermediates, excipients and finished products.
We support customers at various stages of the development/validation process and have a proven track record of success on full development and validation studies, optimization of existing research methods and transfer of previously validated methods.
Whether you need expert testing consultation, method development or validation protocol design, Eurofins BioPharma Product Testing offers the widest range of product testing services in the industry, including:
- Method Development
- Raw Materials and Excipient Testing
- Product Stability and GMP Storage
- Pharmaceutical Release Testing
- Packaging Testing
- Pharmaceutical Gas Testing