Search results for "regulatory"
Article
Traceability in Western Blot Imaging: Considerations for GxP
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Densitometry analysis of gels is a key part of quality control in the pharmaceutical drug release process. In regulated environments, electronic record-keeping can improve both tra…
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Cytiva Webinar Hub
Welcome to the Cytiva webinar hub! Please select content below to watch.
Article
Accelerating an Orphan Therapy to Market
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This case study shares the work of Cytiva’s Fast Trak Services team to help accelerate development of a process for cGMP production of material for toxicology studies.…
Article
Diamyd Medical Selects Cytiva’s FlexFactory Platform to Make Precision Medicine Type-1 Diabetes Vaccine
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Diamyd Medical will install a new Cytiva FlexFactory platform in Umeå, Sweden. Once up and running, the clinical-stage biopharmaceutical company will begin manufactu…
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Meeting the Process Development Challenges of a Diverse Biologic Pipeline
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In the current biopharmaceutical landscape, developers are constantly encountering new and diverse biological molecules with complex structures. While these novel biolog…
Article
mRNA Therapeutics and Vaccines – Key Process Considerations
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Learn more on key considerations and strategies for process development and scaling up in our new web hub for mRNA therapeutics and vaccines.
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Advanced Cell Therapy Technology Fast Trak Course (CELLT1)
This free webinar gives an overview of cell and gene therapy manufacturing and what the current landscape looks like.
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Accelerate Process Development: On-Demand Webcast Series
Accelerate Process Development: On-Demand Webcast Series
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Challenge Analytical Complexity–Biacore SPR Systems
Join on-demand presentation "Challenge analytical complexity" at DiPIA online
Article
The Importance of Process Intensification and PAT for Achieving Real-Time Release
One way to help advance the understanding of new technologies is for instrument vendors to get their new technologies into the hands of the academic, industry, and regulatory science investigators to …