Facility Design Webinars

  1. A State-Of-The-Art Syringe Liquid Sampler 6/24/2025

    Discover a cutting-edge syringe liquid sampler for Life Sciences that offers USP <788> compliance, versatile syringe compatibility, and advanced features for precise particulate testing.

  2. Cleanroom Conceptual Design Paradigm: Converting Spaces For GMP Operations Part 2 6/16/2025

    Learn essential conceptual design principles for transforming alternative spaces into efficient, regulatory-aligned cleanroom environments for your critical processes.

  3. Considerations For Tangential Flow Filtration Process Development 5/27/2025

    Optimize your TFF process with single-pass technology by joining experts Mike Dango and Michael Brauchle as they share key strategies for scalable, efficient filtration process development.

  4. Setup Made Simple With The BioTitan Retention Device 5/27/2025

    Find out how quick and simple it is to set up an assembly secured with the Thermo Scientific BioTitan Retention Device.

  5. An All-In-One Solution For Residual DNA Quantitation 5/22/2025

    Explore an all-in-one solution for residual DNA quantitation with a 3D lab tour with virtual demos, videos, and interactive instrument guides to experience the full workflow.

  6. Bioprocessing Equipment And Automation Product Portfolio Overview 5/19/2025

    Accelerate biotherapeutic development with innovative bioprocessing equipment and automation solutions that feature single-use mixers, bioreactors, and more to streamline workflows and speed products to market.

  7. Facilities And Capital Considerations For Continuous Manufacturing 5/16/2025

    We entertained several audience questions during our recent Bioprocess Online Live event Process Optimization or Full-Scale Automation. In this segment from the virtual event, David Bruehlmann addresses questions about facility considerations for continuous manufacturing, highlighting findings from Amgen and that indicate continuous enabled a considerably smaller facility footprint than batch. Considerations for new facility investment decisions.

  8. PUPSIT Without The Pain: Practical Solutions For Implementation 5/6/2025

    Explore the critical role of pre-use post-sterilization integrity testing in quality risk management, as well as learn about integrity testing, wetting procedures, and innovative filtration systems for effective implementation.

  9. White Raven's Accelerated Path To GMP Certification 4/28/2025

    CDMO White Raven achieved GMP certification using an innovative aseptic filling solution in just 18 months. Discover how meticulous planning and collaboration set a new industry standard for efficiency.

  10. Why Internal Manufacturing Is Key To Meira GTx's Success 4/23/2025

    CEO Zandy Forbes shared Meira’s origin story and how building an in-house manufacturing facility allows the company to develop an expansive pipeline of gene therapies.