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Europe’s leading event for a comprehensive update on operational strategies, technologies, regulatory changes, manufacturing production and process development in biological manufacturing. With 4 streams to choose from, this programme explores best practices in antibody production and downstream processing, the use of disposable systems, Quality by Design and protein characterisation; ensuring you come away with all the tools you need to optimise your biopharmaceutical product development.
More dedicated networking time to provide you with the perfect platform to share your experiences and make new contacts with senior level attendees in one venue over 2 full days.
REGISTER TODAY TO SAVE ££’s, by emailing us at: registrations@informa-ls.com or by phone: +44 (0) 20 7017 7481, quoting CQ3423
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Facility Design Strategies for Single-Use Technologies
Please join us for a free webinar addressing strategies for facility design in biopharmaceutical manufacturing:
Wednesday, 29 February 2012
8:00 AM and 1:00 PM EST
Presented by:
Ingrid Long, MSc
Research Engineer
GE Healthcare Life Sciences
During the webinar, Ms. Long will discuss the impact of different strategies for facility design, with a focus on the following topics:
* Replacement of traditional equipment with the single-use equivalent
* Biopharmaceutical manufacturing in a single room
* Benefits of facility design with respect to cost, risk, and flexibility
Development of a Plant-Made Pharmaceutical Production Platform
Recommendations for Cell Banks Used in GXP Assays
Efficient Aggregate Removal from Impure Pharmaceutical Active Antibodies
Implementation of Single-Use Technology in Biopharmaceutical Manufacturing
Production and Purification of a PER.C6-Expressed IgM Antibody Therapeutic
How QbD and the FDA Process Validation Guidance Affect Product Development and Operations, Part 2