Testing of raw materials, packaging materials, bulk solutions, in-process controls, and finished products for lot release, according to Eur. Ph. or international Pharmacopoeias or Client specifications.
Full range of techniques (microbiology, biochemistry, bioassay, and physical chemistry) for the analysis and characterization of products.
Design and execution of stability studies (pre-register, register, in use, ongoing, forced degradation, etc.).
Complete development, transfer, implementation, and validation of analytical methods to comply with international guidelines.