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Archive for category: General

Single-Use Systems Supply Chain Issues and the Impact of COVID-19

March 16, 2021/in Blog, General /by Ashley Farley
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Best Practices When Assessing Your Bioprocessing Quality Risk Management (QRM) Program

March 4, 2021/in Blog, General /by Ashley Farley
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How to Shorten Validation Document Review and Approval Cycles to Achieve Faster Systems Release

February 23, 2021/in Blog, General /by Ashley Farley
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Challenges of Rapid Growth: Expanding Within Your Footprint

February 18, 2021/in Blog, General /by Ashley Farley
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Latest EU GMP Annex 1 Revisions: What’s New and What’s Next

February 4, 2021/in Blog, General /by Ashley Farley
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“That’s What I Love About ICQ” — Camelia Rodriguez

January 12, 2021/in Blog, General /by Ashley Farley
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How CMOs Can Ensure a Smooth IND Application for Biotech Clients

November 19, 2020/in Blog, General /by Ashley Farley
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Game, Set, Batch: Was 2020 the Catalyst for a Widespread Shift to Continuous Processing?

November 9, 2020/in Blog, General /by Ashley Farley
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An Introduction to Commissioning and Qualification

August 27, 2020/in Blog, General /by Ashley Farley
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5 Ways to Avoid Data Integrity Issues for Improved Quality

July 22, 2020/in Blog, General /by Ashley Farley
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From the Blog

  • CQV Tips for Cell & Gene Therapy CDMOs at Each Phase of ConstructionApril 1, 2021 - 8:00 am
  • Single-Use Systems Supply Chain Issues and the Impact of COVID-19March 16, 2021 - 8:00 am
  • Best Practices When Assessing Your Bioprocessing Quality Risk Management (QRM) ProgramMarch 4, 2021 - 8:00 am

Executive Briefs

  • A CQV Checklist for Gene Therapy Facilities
  • A Pragmatic Approach to Biopharma Commissioning, Qualification, and Validation

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