What is a Certificate of Analysis (COA)?

17.02.2025

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A document containing the name and address of the laboratory performing the test(s), name and specifications of the material(s), test(s) performed, test method(s) used, actual numerical results, approval date(s), signature of approver, and any other technical information deemed necessary for its proper use. [Canadian GMP Guidelines 2018]

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24.11.2025

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How is a QRM process initiated?

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FDA: Updated Pre-RFD Guidance for Combination Products

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EDQM: 9 Virtual Training Modules on Ph. Eur. and CEPs

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