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Abstract: 

Designing a Single-Use Biopharmaceutical Process, 2p.

Abstract: 

Evaluating the Rewards vs. the Risks of Automation, 5p.

Abstract: 

Expansion in Cell Culture Facility Offerings, 3p.

Article: 

Analysis of Residual Impurities in Continuous Manufacturing

Article: 

Best Practices in the QC Micro Laboratory

Article: 

Can Nanotechnology Deliver Big Drug Benefits?

Article: 

Can Policy Keep Pace with Science and Discoveries? The promise of new therapies is tempered by the need for affordability, safety, and ethics.

Article: 

Can Vaccine Development Be Safely Accelerated?

Article: 

Contamination Control for Cell Therapy

Article: 

Design Considerations for a Commercial Cell and Gene Therapy Facility

Article: 

Flexible Facilities for Viral Vector Manufacturing

Article: 

Managing Biologic Equipment Cleaning

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More Predictable Post-Approval Change Policy on Horizon, 2p.

Article: 

Moving From Compliance to Quality

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Prepping Fill/Finish Systems to Ensure Quality Output

Article: 

Seeing Success with Single-Use Solutions

Article: 

Taking Stock of Biologic Fill/Finish Best Practices

Article: 

Taking Therapeutic Antibodies to the Next Level

Article: 

The Case for Stainless Steel

Article: 

The Case for Stainless Steel

Article: 

The Case for Stainless Steel

Article: 

What’s New in Downstream Processing