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Master Series: What to Expect and How to Address Data Integrity Audits

March 11, 2020 By Rapid Micro Biosystems

New FDA regulations have put concerns about Data Integrity in QC micro labs and pharma manufacturing front and center. In response, Rapid Micro..

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5 Steps To Selecting The Appropriate Statistical Test During RMM Validation

February 27, 2017 By Admin User

Regulators at the Food and Drug Administration (FDA) and European Medicines Agency (EMA) demand that the industry prove equivalence between RMM..

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