Resources

White Papers

Resources

White Papers

Overcoming Challenges of Rapid Growth

How to Conquer Four Major CQV Obstacles

Achieving Organization-Wide Integrated Commissioning, Qualification, and Validation Activities

Practical, Proven Strategies That Drive Efficiency

The State of the Biopharma Contract Manufacturing Industry

Assessing the Impact of COVID-19, Industry 4.0 and Flexible Design
Ensuring Good Manufacturing Practices for Cell & Gene Therapies
Guide to Maintaining Validation of Older Facilities

Guide to Maintaining Validation of Older Facilities

Why, When and How
How to Prevent a Significant Source of 483s and Warning Letters in Drugs, Devices, and Biologics

Data Integrity: How to Prevent a Significant Source of 483s and Warning Letters in Drugs, Devices, and Biologics

5 Practical Ways to Proactively Avoid Data Integrity Issues for Improved Quality