Transitioning from GCLP to GMP: 4 Considerations to Make

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