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Application of Quality Risk Management to Process Validation
Robert Dream, Managing Director, HDR Company LLC
A Holistic Phase Appropriate Strategy for HCP-Limits and HCP Characterization
Dr. Markus Haindl, Global Head Gene Therapy Technical Research & Development, Roche Di...
Strategies for Extractable and Leachable Risk Assessment of Polymeric Single Use Systems U...
Ping Wang, Director, Johnson & Johnson
Use of Non-Contact Raman Spectroscopy to Derive Reaction Kinetics
Richard Hart, Senior Director – Head of Automation and Data Science (Previously Asso...
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Navigating Technology Transfer
Overcoming Obstacles in AAV Viral Vector Manufacturing
Benefits of Mixed-Mode Cation Exchange Chromatography: CMM HyperCel™ Sorbent Used for Monoclonal Antibody and Other Recombinant Protein Purification
Enabling Total Biopharma Solutions
Pall Life Sciences
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Viatris agrees to acquire Pacira BioSciences for $1.65 billion to add Exparel and Zilretta
Astellas to present 21 oncology abstracts at ESMO 2026, with long term PADCEV plus pembrolizumab bladder cancer data and zolbetuximab research in gastric cancer
Efzimfotase alfa misses statistical significance on primary walking endpoint but improves fatigue in adolescents and adults with hypophosphatasia in HICKORY Phase III trial
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Upcoming Webinars
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The Business Benefits of PAT in Continuous Drug Product Manufacturing
Presented by Steve Hammond, Independent Consultant at Steve Hammond Consulting
22nd September 2021
Towards a lean Manufacturing: Implementing Single-Use Process Analytical Technologies (PAT) tools at the seed stage to simplify cell culture operations
Presented by Dr Jose R. Vallejos of Medimmune/AstraZeneca
24th May 2017
Future Trends To Control Risks From Extractables and Leachables
Presented by Jason Creasey, Managing Director at Maven E&L Ltd and Kathleen Lava PhD – E&L Expert Nelson Labs Europe
09th February 2021
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At Pall we help you select the process model that’s perfect for you. Ensuring it’s adapted to meet your precise needs and assembled flawlessly, ready for the future, from day one.
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Best Practices for Achieving Virus Safety
Strategy Emerging Markets for Risk Mitigation
Amsphere TM A3
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Decrease Cleaning Validation Time and Resources
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