Regulatory Compliance Videos
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Cell Therapy Process Development Made Easy
3/27/2024
Explore how Fast Trak™ process development services offered by Cytiva can guide you through achieving GMP compliance in your cell therapy manufacturing process.
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Challenges Associated With Building New Isolator Technology
3/26/2024
Paula Rizo, Germfree’s Mechanical Engineering Lead for Equipment, dives deeper into our collaboration with AST and how this isolator technology will transform the way pharmaceutical companies approach aseptic processing.
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Single-Use Strategies For Uninterrupted Microbial Monitoring
2/22/2024
Watch as Emad Albarouki, a microbiology and sterility assurance specialist at Particle Measuring Systems, discusses the best practices for using BioCapt® Single-Use in continuous microbial active air monitoring.
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What Indications Can, And Will, mRNA Therapeutics Address?
12/5/2023
During our Bioprocess Online Live event, mRNA Update: Beyond Prophylactic Vaccines, we asked an audience of several hundred biopharma professionals what indications they’re addressing in mRNA therapeutic development. Here, our panelists address their responses and offer final thoughts on unfolding mRNA regulatory frameworks.
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Safety & CQAs: Do mRNA Therapeutic Regulators Know What They Want?
12/5/2023
In this segment, Combined Therapeutics CSO Thomas Van Cott, Ph.D. and Omega Therapeutics Executive Director, Process Development and Analytical Sciences Jeff Atkinson, Ph.D. address regulators’ likely safety and CQA concerns as well as audience questions regarding variable and changing RNA constructs.
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US GMP (21 CFR 820) Manufactured Oligos For Preclinical Research
10/18/2023
Learn why Custom cGMP Oligos should be considered to ensure oligo products meet the strict standards of MDx, LDTs, and preclinical research.
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How To Evaluate The Integrity Of Intravenous (IV) Bags
7/7/2023
Testing IV bags in compliance with Annex 1 guidelines requires a robust technology strategy to ensure product quality and patient safety. Learn how to deploy and validate technologies for IV bag CCI.
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An Efficient And Reliable Way To Digitalize Your Sterility And QC Testing Data
5/2/2023
Watch to learn about the M-Trace™ Electronic Test Record Software, your digital QC companion for trusted and efficient data recording that automizes and digitalizes your sterility and QC testing data.
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Simplifying Bioprocess Data Collection
2/17/2023
Centralized bioprocess data collection and aggregation lowers the risk of data loss during any manual retrieval process. Discover a solution that helps you meet data storage and reporting requirements.
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3-Bucket Mopping System - Correct Mopping Protocol
12/9/2022
Discover the proper mopping techniques when using a 3-bucket system through an in-depth demonstration and detailed instructions.