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USP Qualification of Chemical Entity for Clinical Trial
Looking to qualify a research grade chemical entity, 98% purity with CoA, as a raw material that meets USP standards as an key ingredient within a finished product under GMP for topical application within a clinical study.
Members of our Laboratory Outsourcing Network can use our online platform to communicate with the Lab Requestor, submit responses with quotes and have access to more information such as budget, location required, etc.
Contract Laboratory can help you with all your Pharmaceuticals testing, analysis, scientific research and development, inspection, certification, engineering, failure investigation, and product development needs including:
Need Pharmaceuticals Testing or Scientific Research?
Save time and money searching. Simply, submit a Pharmaceuticals request to find the laboratories or lab suppliers that best meet your needs.
Pharmaceutical Analytical Chemistry Laboratory needed for USP Inulin Monograph testing for free Fructose, Content of com... view
FDA GMP / GLP Pharmaceutical Analytical Laboratory needed Development and validation of the dissolution method with the ... view