Regulatory Compliance Videos

  1. The Future Of GxP Manufacturing With AI 4/21/2025

    Discover how to digitize batch records in just 180 days with Christian Gay Porcel by leveraging AI for automated compliance and scalable validation.

  2. Revolutionizing Aseptic Fill-Finish With Innovation 4/21/2025

    Experience an innovative aseptic fill-finish technology designed for ATMP production in this live demo, which is a cutting-edge solution that ensures optimal efficiency and product quality.

  3. Adopting Isolators To Overcome Aseptic Challenges With ATMP Processing 4/21/2025

    Gain insight into how Isolators enhance ATMP production by providing superior control and protection to ensure compliance with GMP regulations and to reduce cleanroom costs.

  4. MilliporeSigma Bio-Expo Live February 2025: Upstream Bioprocessing 3/18/2025

    Review the benefits of implementing a closed and sterile sampling system, such as NovaSeptum®, to improve sampling procedures and meet regulatory expectations.

  5. Kneat Solutions Bio-Expo Live February 2025: Quality, Data, And Analytical Solutions 3/17/2025

    Discover how top pharma companies streamline validation, reduce cycle times by 40%+, and ensure compliance with a digital validation platform that also aids in real-time reporting and compliant testing.

  6. ETQ Bio-Expo Live February 2025: Quality, Data, And Analytical Solutions 3/17/2025

    Discover how a flexible eQMS ensures compliance with evolving regulations, reduces compliance issues, and keeps your organization audit-ready while driving continuous improvement in any economic or market conditions.

  7. Environmental Monitoring For Aseptic Filling 3/6/2025

    Explore regulatory interest in modern environmental monitoring for aseptic filling, the benefits of biofluorescent particle counters, and their role in enhancing drug product safety and quality.

  8. Different Clean Room Regulations For Peptides 2/11/2025

    Clean room requirements for peptide production can vary based on the manufacturing process. For example, recombinant expression carries a higher risk for contamination than chemical synthesis. In this segment from the Pharmaceutical Online Live event, "Opportunities For Innovation In Peptide Manufacturing," our panelists discuss the importance and need for clarity and guidance around peptide clean room requirements.

  9. 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.

  10. Building A Strong Safety Culture In The Biopharmaceutical Industry 1/25/2025

    Explore how fostering a strong safety culture — rooted in accountability, collaboration, and proactive risk management — can drive operational excellence and long-term success in biopharmaceuticals.