MilliporeSigma Webinars

  1. Get Your Aseptic Facility Ready For EU GMP Annex 1 7/21/2022

    Here, we review contamination control strategy (CCS) considerations, the setup of a microbiological environmental monitoring program, and how to optimize the design of hardware and consumables for specific environments.

  2. The Future Of Robotics And Automation In QC In Microbial Testing Labs 4/7/2022

    Automation based on the use of robotics and digital tools will transform the QC process in microbial testing labs to meet the productivity, data integrity, and reliability requirements of Pharma 4.0.

  3. Maximizing Safety In The Daily Handling Of Hazardous Goods In The Lab 4/7/2022

    Understand the role of safety in the lab as well as the challenges of handling hazardous goods and how you can overcome them.

  4. Assess Pyrogenic Risk With The Monocyte Activation Test 2/5/2021

    Microbial risk in pharmaceutical processing cannot be limited to viable microorganisms. Learn how the MAT can help you to assess the pyrogenic risk resulting from your production process.

  5. Bioburden And EU GMP Annex 1: Risk Assessment, Reduction, And Testing

    Experts on regulation, filtration, sampling, and quality control discuss risk assessment and filtration-based strategies to reduce bioburden.

  6. Key Challenges When Selecting Media For Media Fill Tests

    In this 10-minute quick learning tutorial, an expert will guide you through the main challenges for aseptic manufacturers when selecting a medium for media fill tests or aseptic process simulations.

  7. Single-Use Technology For Quality mRNA Manufacturing

    Learn how single-use technologies deliver important benefits for mRNA manufacturing, including increased speed, quality, flexibility, and adaptability to different dosages and scale-up strategies.

  8. Selecting The Right Media For Your Aseptic Process Simulations

    Media fill experts from MilliporeSigma provide an overview of what to consider when selecting media for aseptic process simulations, particularly regarding regulatory requirements and user requirement specification (URS).

  9. Making Sense Of Analytical Standards In Pharma QC

    Reference materials are a critical component of the analytical testing workflow. Learn about metrological traceability, the hierarchy of reference materials, fit-for-purpose selection considerations, and more.