Regulatory Compliance Videos

  1. Reducing Costs, Making Peptide Synthesis Greener 2/11/2025

    Greenness is the measure of a process's environmental impact (based on raw material use and waste) and efficiency. In this segment from the Pharmaceutical Online Live event, "Opportunities For Innovation In Peptide Manufacturing," our panelists discuss ways to improve process efficiency and save on material costs, e.g., by reusing solvents in washing steps or making a shift towards more recoverable solvents.

  2. Comprehensive Regulatory Support 8/29/2024

    Review our expertise across a wide range of global markets. Our experience in securing regulatory approvals and navigating market challenges positions us as a trusted partner.

  3. Overview Of Biological Indicator And Sterilization Monitoring Systems 7/2/2024

    Watch to explore the use and proper placement of biological indicators in hydrogen peroxide decontamination processes.

  4. Cleanroom Classification Zone Creation For ISO 14644, Annex 1, China GMP 6/11/2024

    Discover a particle counter that automatically determines the number of sample locations needed based on the sampling size of the area, enabling the easy selection of classification for certification.

  5. Just Press Start To Begin Manually Counting Particles In Your Cleanroom 5/6/2024

    With the press of a button, you can immediately start taking particle counts in your cleanroom using a portable particle counter for easy cleanroom monitoring.

  6. How To Easily And Quickly Monitor Cleanrooms 5/6/2024

    Discover a portable particle counter for quick and easy cleanroom monitoring that features automated alarms and reporting to help you ensure compliance.

  7. How To Do Quick, Easy Cleanroom Classification 5/6/2024

    Classification plays a vital role in cleanroom certification and qualification. Discover a particle counter that simplifies testing for adherence to ISO 14644-1, EU GMP Annex 1, or China GMP standards.

  8. Process Liquids And Buffers Offering 5/2/2024

    Whether you are a researcher, scientist, or industry professional, this video will provide valuable insights into our large volume liquids manufacturing capabilities.

  9. Gain Support For Your Regulatory Submission Process 3/27/2024

    Join us in this video as we delve into invaluable tips, cutting-edge tools, and unwavering support that Cytiva offers to facilitate your documentation progress.

  10. 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.