Getting your investigational drug regulatory ready
December 1, 2023 - Cytiva
Navigating regulatory requirements can be an o
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Democratizing GMP Manufacturing for the New Therapeutic Pipeline
December 1, 2023 - BioPharm International
PharmTech Europe
discusses technology that enable
Developing oligonucleotide therapeutics with confidence
November 17, 2023 - Cytiva
In this video, we will look at
Good modeling practice: workflow and case study
November 17, 2023 - Cytiva
Learn more about a recommended mechanisti
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Top challenges in recombinant protein purification process develo
November 17, 2023 - Cytiva, BioPharm International
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Discussing the Origins of the mRNA Therapeutics Field
November 17, 2023 - BioPharm International
Andy Geall, co-founder and chief development officer at Replicate
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Chromatography processes for the diversified therapeutic antibody
November 3, 2023 - Cytiva
The diversity of antibody variants in today’s pipeline presents unique challenges for purification and we see molecules such as bsAbs, Fabs, dAbs, and others.
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Process Development for Viral Vectors
November 3, 2023 - Cytiva
Scaling viral vector processes can be challenging, but it doe
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Digitalization: The Route to Biopharma 4.0
November 3, 2023 - BioPharm International
Efficient and Scalable Buffer Preparation
November 3, 2023 - Cytiva
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