Quality control is essential for ensuring that drug products are marketed safely and effectively. From drug development and manufacturing through finished product, Eurofins Lancaster Laboratories routinely performs QC analysis according to cGMP quality standards for Active Pharmaceutical Ingredients (APIs), bulk drugs, intermediates, excipients, finished products and packaging components.
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 Lancaster Laboratories offers the widest range of product testing services in the industry, including:
- Method Establishment
- Raw Materials and Excipient Testing
- Product Stability Testing & Storage
- Packaging Testing
- Pharmaceutical Release Testing
- Biopharmaceutical Release Testing
- Viral Safety Testing
- Lot Release Testing