Prepare for an FDA Bioburden Inspection

BioPharm presents the Process Development Forum | Sponsored by GE Healthcare

New This Week on Process Development Forum

Prepare for an FDA Bioburden Inspection
Former FDA inspector and Biologics License Application reviewer shares her expert tips.
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Connected Polishing and Concentration Under One Automation Method
This work aims to demonstrate the capability of the UNICORN™ system control software to integrate unit operations and eliminate intermediate hold steps.
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Reducing Cross-Contamination Risks in Process Chromatography
Single-use systems provide replaceable fluid paths.(Read Article)

Roadmap Leads to Innovative Biomanufacturing Strategies
The Biomanufacturing Technology Roadmap is accelerating innovative manufacturing strategies for biopharmaceuticals.
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Process Development Forum Topic Spotlight

QbD: Reliability Rooms and the Move to Proactive Supply Chain Management

Biosimilars: Multidimensional Scale-up of a Monoclonal Antibody Capture Step, Using ÄKTA™ Pilot 600

HTPD: ADC Development Robust Despite Lackluster Performance

Process Development: Start with the End in Mind: GMP Tech Transfer

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