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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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New Paper Describes the Simplified Validation Process of Growth Direct for In-Process Microbiological Testing

February 26, 2018 By Rapid Micro Biosystems

In-process microbiological testing can be both time-consuming and labor-intensive for the micro QC department. Reducing the Time to Result (TTR)..

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