milliporesigma videos

  1. Enhanced API Solubility And Stable, High Drug Loads
    4/12/2017

    Poor solubility of APIs is a critical challenge in drug development. One formulation technique to address this challenge is hot melt extrusion.

  2. How To Best Manage And Remove Aggregates From Your mAb Process?
    2/14/2017

    Aggregates in mAb therapeutics pose a risk to patients. Are you considering how best to manage and remove aggregates across your template?

  3. Overcoming Drug Development Regulatory Challenges: The Emprove® Program
    2/14/2017

    Introducing a new drug to the market is an extensive and intricate process. Development, testing, and registrations take years to complete after a new patent has been commissioned. Expediting approval preparation and maintaining reliable manufacturing processes are crucial for a quick market launch. That’s why MilliporeSigma devised the Emprove® Program. In this video you will learn how this program supports risk assessment and offers assistance in developing more robust processes.

  4. Process Development Resource: M Lab™ Collaboration Centers
    2/13/2017

    The M Lab™ Collaboration Centers are resource hubs to explore ideas, learn innovative techniques, and collaborate to find solutions to your unique process development challenges, big and small. Our process development scientists specialize in and partner with you on upstream, downstream, and final fill challenges at nine non-GMP facilities around the world.

  5. Overcoming Regulatory Challenges: Emprove® Regulatory Dossiers For Chemicals
    2/2/2017

    This video provides information on how the dossiers of the Emprove® Program support throughout the different stages of operations: Qualification, Risk Assessment and Process Optimization, with a focus on pharma raw and starting materials.

  6. Overcoming Regulatory Challenges: The Emprove® Program
    2/2/2017

    Introducing a new drug to the market is an extensive and intricate process. Development, testing, and registrations take years to complete after a new patent has been commissioned. Expediting approval preparation and maintaining reliable manufacturing processes are crucial for a quick market launch.

  7. Reliable And Validated Connections For Multiple Transfers Of Sterile Fluids
    11/9/2016

    The Lynx® CDR (Connect, Disconnect and Reconnect) device provides a reliable and validated connection for multiple transfers of sterile fluids.

  8. Tentacle Ion Exchange Chromatography Animation: How It Works
    10/25/2016

    We’ve created a short animation, for demonstration purposes only, to explain our unique resin tentacle technology and the enhanced performance of our tentacle ion exchangers over conventional chromatography resins. Watch our animation today to see for yourself how our tentacle chromatography technology can benefit your downstream protein purification process.

  9. CHO Cell Line That Is Resistant To Infection Minute Virus of Mice (MVM)
    10/13/2016

    MilliporeSigma has identified a gene target (Slc35A1) that, upon elimination of expression by gene editing, results in a CHO cell line that is resistant to infection by Minute Virus of Mice (MVM). 

  10. Achieve Greater Bioprocessing Efficiency And Productivity
    9/6/2016

    MilliporeSigma also evolved from manual assembly to automation with a focus on achieving greater process efficiency and productivity.