QCL provides cGMP contract analytical, stability, synthesis, and microbiological testing services to pharmaceutical companies worldwide.

We support all phases of pharmaceutical product development and commercialization. Our customers appreciate the responsiveness, customer service, and quality. Capabilities include analytical method development and validation, drug product and API testing, ICH stability storage and testing, impurity isolation/characterization/synthesis, API process development with mg to kg GMP synthesis, raw material testing (USP, BP, EP, ACS, FCC, vendor methods), and comprehensive microbiology services. ...

We support all phases of pharmaceutical product development and commercialization. Our customers appreciate the responsiveness, customer service, and quality. Capabilities include analytical method development and validation, drug product and API testing, ICH stability storage and testing, impurity isolation/characterization/synthesis, API process development with mg to kg GMP synthesis, raw material testing (USP, BP, EP, ACS, FCC, vendor methods), and comprehensive microbiology services. Located in Wilmington, NC, QCL has over 47,000 sq. ft. of FDA and DEA registered facilities with 12,000 cubic feet of ICH compliant stability storage conditions.