QCL is under Licence with Health Canada (Licence No. 101432-A) and Registered with U.S. Food and Drug Administration, FDA (Registration No. 3005630028). QCL offers a significant range of analytical testing services supporting pharmaceutical, biotechnology and related industries. Laboratory resources provide analytical support for Drug Research, Formulation Developments, Clinical Trials, Production, API's and Finished Products Release phases.

Our expertise includes routine and non-routine Analytical Testing, Quality Control, Trouble-shooting, Method Development and Validation, and Stability Studies for a wide range of applications and situations. Analyses are performed as per industry standard compendial methods such as; USP, BP, EP, JP, etc. as well as in-house and client's validated methods. The analytical testing at QCL are compliant to Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) standards.