Archive for category: General

How to Accurately Staff Validation Projects

Growing and Innovating: The State of U.S. Biopharma Contract Manufacturing

The Cleanroom of the Future: What to Expect

Facility Qualification in Pharmaceuticals

COVID-19 Has Shaped the Future for Biopharma: How to Stay Ahead

What You Need to Know About a Risk-Based CSV Approach

Challenges of Rapid Growth: Scaling Validation Processes

Ensuring Good Manufacturing Practices for Cell & Gene Therapies

A 10-Point Checklist for Cell & Gene Therapy Facility CQV

Designing Flexibility into CGT Facilities: The CQV Advantages

That’s What I Love About ICQ

“That’s What I Love About ICQ” – Alex Khaw

hydrophobic filters

Know the Difference Between the Three Main Filter Integrity Tests

About ICQ

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