Automation Trend in Fill/Finish Reduces Contamination Risk
June 21, 2018 - BioPharm International
Aseptic fill/finish is crucial in biopharma manufacturing and is optimized through automated technology.
By Feliza
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Understanding Validation and Technical Transfer, Part 2
June 21, 2018 - BioPharm International
Understanding Validation and Technical Transfer, Part 2
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Understanding Validation and Technical Transfer, Part 3
June 20, 2018 - BioPharm International
Understanding Validation and Technical Transfer, Part 3
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Establishment of New Modern Plasma Fractionation Facilities in As
June 19, 2018 - Process Development Forum
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Achieving Efficient Adenovirus Upstream Production
June 7, 2018 - Cytiva
Adenovirus is one of the most frequently used viral
Get Acquainted with How SPR Technology is Used for Better Protein
June 7, 2018 - Cytiva
Surface plasmon resonance (SPR) has become a go
Optimization of Adenovirus Midstream Purification Steps
June 7, 2018 - Cytiva
Adenovirus (AdV)-based vectors are widely evaluated a
Web Chat June 19: Challenge Cytiva Scientists with Multistep Puri
June 7, 2018 - Cytiva
Automated multistep (or multidimensional) protein purification is used to free up time, increase throughput, and reduce intermediate sample storage.
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Putting Viral Clearance Capabilities to the Test
June 7, 2018 - BioPharm International
Process understanding and careful assessment of risks are essential in developing viral clearance programs.
CDMOs Driving Emerging Bio/Pharma Success
June 7, 2018 - BioPharm International