Search results for " QbD"
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Cytiva Webinar Hub
Welcome to the Cytiva webinar hub! Please select content below to watch.
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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.…
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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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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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Getting Your Investigational Drug Regulatory Ready
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Navigating regulatory requirements can be overwhelming. This article outlines basic strategies for efficient regulatory review and drug approval.
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Planning for IND
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Learn how to navigate regulatory requirements as you progress through clinical trials to commercialization.
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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
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Updating Viral Clearance for New Biologic Modalities
Viral clearance processes and guidance must evolve along with newer biotherapeutic modalities.
By Feliza Mirasol
Ensuring viral clearance (i.e., removal) in downstream purification has becom…