Search results for "qbd"

Resource Cytiva Webinar Hub
Welcome to the Cytiva webinar hub! Please select content below to watch.

Article Accelerating an Orphan Therapy to Market
Click here to learn more >> 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
Click here to learn more >> Diamyd Medical will install a new Cytiva FlexFactory platform in Umeå, Sweden. Once up and running, the clinical-stage biopharmaceutical company will begin manufactu…

Article mRNA Therapeutics and Vaccines – Key Process Considerations
Click here >> Learn more on key considerations and strategies for process development and scaling up in our new web hub for mRNA therapeutics and vaccines.

Article Getting Your Investigational Drug Regulatory Ready
READ FULL ARTICLE >> Navigating regulatory requirements can be overwhelming. This article outlines basic strategies for efficient regulatory review and drug approval.

Article Planning for IND
Click here to read more >> Learn how to navigate regulatory requirements as you progress through clinical trials to commercialization. 

Resource 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.  

Resource Accelerate Process Development: On-Demand Webcast Series
Accelerate Process Development: On-Demand Webcast Series

Resource Challenge Analytical Complexity–Biacore SPR Systems
Join on-demand presentation "Challenge analytical complexity" at DiPIA online

Article 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…

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