Method Development and Validation QCL offers analytical method development and validation services for Active Pharmaceutical Ingredients (APIs), Drug Production Formulations, cleaning agents used in manufacturing processes, and raw materials/excipients. The dedicated group of chemists that perform these studies have many years of experience in such disciplines as HPLC, GC, ICP, AA and Dissolution. All method validations are performed under cGMP requirements and meet the current ICH and FDA guidelines.
Raw Materials Analysis QCL offers a 10-day turnaround time on all raw materials testing. This applies to USP, EP, JP, BP, FCC, ACS, and client-supplied methods. For all compendial purified water testing, QCL offers a 5-business day turnaround time. QCL's dedicated group of experienced chemists allows us to offer this exceptional turnaround time.
3400 Enterprise Drive
Wilmington , NC 28405 US