MilliporeSigma Webinars

  1. Turnkey Solutions For Upstream Cell Culture Processes 1/19/2022

    Learn about the benefits of a one-step and neutral pH feed optimization strategy, the potential application of chemically defined hydrolysates, and supplements targeted at adjusting glycosylation attributes.

  2. Getting It Right. A Candid Conversation About Remote Viral Clearance Studies 8/19/2021

    Evolving regulatory guidelines and a global pandemic will not derail your viral clearance study timelines with Provise™ Clearance services.

  3. Advancing Biopharm Manufacturing And Supply Chain Capabilities With An Integrated eData Solution 4/13/2021

    This webinar describes how the implementation of Pharma 4.0 technologies across the industry offers the promise and opportunity to significantly improve many aspects of Biopharma manufacturing and supply chain capabilities. eData exchange is a critical aspect of realizing the full potential of these digital solutions.

  4. How Biosafety Assurance Can Be Both Rapid And Purposeful 2/24/2021

    A discussion on how novel treatment modalities such as viral vectors and the urgent need for SARS-CoV-2 treatments and vaccines are driving the advance of biopharma. 

  5. Effect Of Product Concentration On Continuous Parvovirus Retentive Filtration 2/23/2021

    This video illustrates how careful process development and system design can address higher-concentration intermediate challenges and optimize virus filtration processes.

  6. Evaluating Viral Clearance For Continuous Processes 10/18/2020

    Is viral clearance a hurdle to implementing continuous processing? Here we share virus spiking alternatives that may pave the way for evaluating viral clearance by chromatography steps.

  7. A Single-Use, Integrated mAb Biosimilars Purification Platform 10/10/2019

    In biopharma, there's a shift toward higher productivity processes resulting in improved economics without compromising quality. Integrated continuous production technologies are gaining interest. 

  8. Mitigating Risk Through Product Characterization 7/17/2019

    In this webinar, multiple approaches to characterizing the physico-chemical and structural attributes of therapeutic mAbs is presented with a focus on how it influences the resulting biological activity.

  9. How Molecular Structure Influences Potency Of A Therapeutic Biologic 7/17/2019

    Gain an understanding of how an antibody’s molecular structure and its many measurable properties influences its binding and affects potency of a therapeutic biologic.

  10. Current Regulatory Expectations And Technical Advances In The Quality Control Of Biological Medicinal Products 10/23/2018

    This webinar describes a number of topics in the areas of cell line characterization and bulk harvest testing for contaminants where new technical innovations are occurring. The regulatory response to these developments is also discussed.