Date :
Place : United States of America, Boston
Website :http://go.evvnt.com/2741227-0?pid=80
Contact Person:Lara Chick
Description:
Troubleshoot Potency Assay Development, Determine Required Reference Standard Material and Implement Potency Assurance to Meet New Regulatory Requirements for Cell Therapies. Time: 8:00 AM - 5:00 PM. Prices: USD 2599.00 - USD 5097.00.Deadline for abstracts/proposals : 11th March 2025
Organized By :
Keynote Speakers :
Conference Highlights :4th Cell Therapy Potency Assay Summit | March 11-13, 2025
Attend the 4th Cell Therapy Potency Assay Summit to connect with industry leading companies in analytical development, cell processing, regulatory, process development, flow cytometry and more!
Troubleshoot Potency Assay Development, Determine Required Reference Standard Material & Implement Potency Assurance to Meet New Regulatory Requirements for Cell Therapies
Troubleshoot Potency Assay Development, Determine Required Reference Standard Material & Implement Potency Assurance to Meet New Regulatory Requirements for Cell Therapies
Establish Mechanism of Action, Quality Control & Regulatory Compliance
In the ever-evolving cell therapy landscape, the challenge of potency assay development remains critical. With the field anticipating finalized regulatory guidelines from the FDA, the need to link mechanisms of action to potency assays scientifically has never been more urgent.
At the4th Cell Therapy Potency Assay Summit, we unite analytical development, quality control, and regulatory experts to tackle these pressing issues. Our goal is tocollaboratively design robust potencyassaysthat not only conform to changing guidelines but also streamline patient access to the next generation of cell therapies.
Check the event website for more details.