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Plasma Product Biotechnology Conference
The sessions, compiled from submitted presentations, will cover the areas of manufacturing, quality, regulatory, pathogen safety, clinical development and technical innovations, and will chaired by re…
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Protein A Fiber Chromatography from Research to Scale-up and Manufacturing of Monoclonal Antibodies
This makes the pre-packed, small-scale Protein A fiber unit a versatile tool for processes such as clone selection and upstream cell-culture media development. The time savings in downstream processes…
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PepTalk: The Protein Science Week
Now, in its 18th year, PepTalk features renowned speakers from academia, biotech and pharma who bring global expertise and perspective to the forefront. The international delegation of over 1,300 part…
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DiPIA 2021 virtual conference
Get inspired by leading experts in academia and industry
Learn tips and tricks in biophysical characterization
Join our scientific discussions
Explore the latest accomplishments in S…
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Bio-Process Systems Alliance
BPSA facilitates education, sharing of best practices, development of consensus guides and business-to-business networking opportunities among its member company employees.
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Accelerate mAb Process Development with Fibro Rapid Cycling Chromatography
In this webcast, Cytiva experts discuss how you can speed up process development with HiScreen Fibro™ PrismA rapid cycling chromatography, including topics like lifetime studies and effective evaluati…
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World Health Organization
It is responsible for providing leadership on global health matters, shaping the health research agenda, setting norms and standards, articulating evidence-based policy options, providing technical su…
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Parenteral Drug Association
Founded in 1946 as a nonprofit organization, PDA is committed to developing scientifically sound, practical technical information and resources to advance science and regulation through the expertise …
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Continuous Biomanufacturing: Achievements and Challenges for Commercial Implementation
The goal is to provide an electric forum to work together in advancing the technical need and operational strategy for implementing continuous manufacturing in pharma industries
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FDA’s Adverse Event Reporting System (AERS)
The FDA uses AERS to monitor for new adverse events and medication errors that might occur with these marketed products.