Life Science Webinars

  1. Monocyte Activation Test: The In Vitro Pyrogen Test For Pharmaceutical Batch Release 2/5/2021

    Used to detect a broad range of pyrogens in parenteral products including pharmaceuticals, biopharmaceuticals or medical devices, the monocyte activation test (MAT) provides an in vitro alternative to conventional animal testing methods in accordance with regulatory guidelines. Want to know more about in vitro pyrogen detection? Discover the benefits of the ready-to-use Monocyte Activation Test kit, learn how to use it, and examine a real-life case study.

  2. Assess Pyrogenic Risk In Pharmaceutical Process With The Monocyte Activation Test 2/5/2021

    Microbial risk in pharmaceutical process cannot be limited to viable microorganisms. Learn how the MAT can help you to assess the pyrogenic risk resulting from your production process. The monocyte activation test (MAT) provides an in vitro alternative to conventional animal testing methods in accordance with regulatory guidelines.

  3. Advances In Cell And Gene Therapy Analytics - How To Use Maurice To Characterize AAVs And LNPs 2/3/2021

    Learn how Maurice can be used to measure surface charge of an LNP-based mRNA vaccine for confirmation of LNP identity in a manufacturing setting, and for stability assessment for process and formulation development. You will also learn how to assess purity, stability and concentration of AAVs.

  4. Application Of Next Generation Analytical Tools For Vaccine Development 2/3/2021

    In this webinar, we provide concise technical overviews of relevant platforms and specific examples of the roles automated analytical technologies play in the vaccine development workflow.

  5. Next-Gen, Cloud-Based Architecture For Centralized Process Data Analytics 2/2/2021

    Explore the advantages of cloud-based software in manufacturing data management and how to cost effectively scale your IT infrastructure to improve productivity, economic growth and sustainability.

  6. Best Practices: Establishing Data Visibility Across Sponsor/CMO Networks 2/2/2021

    In this webinar industry leaders identify novel ways to collaborate and improve adherence to cGMP requirements and ensure compliant quality production. Learn how you can establish reasonable expectations for data transparency and sharing in Sponsor/CMO relationships to ensure effective data management across the supply chain.

  7. Best Practices: Using Validatable Software To Support CPV (Continued Process Verification) And Tech Transfer 2/2/2021

    In this webinr a panel of experts  share their technology transfer, CPV, and validation experiences with and without the support of software. Discover how digital systems help overcome operational and regulatory hurdles through the sharing of accurate and timely product and process knowledge between development and manufacturing teams and across manufacturing sites.

  8. Best Practices: Ensuring Process Data Integrity Throughout The Product Life Cycle 2/2/2021

    In this webinar a panel of experts from discuss how now more than ever the bio/pharma industry needs to adopt strategies to improve the gathering, analysis, reporting and sharing of process data to establish indisputable integrity and improve decision making.

  9. Using Advanced Analytics In Pharma & LIfe Sciences 2/1/2021

    Pharmaceutical companies must thrive in a challenging business environment defined by regulations, competition, and operational excellence. Learn how advanced analytics can help pharmaceutical and life sciences companies gain insight to important data. This webinar will demonstrate how Seeq enables the integration of myriad data sources for rapid investigation and insight to drive improved decision-making.

  10. Effective Pharmaceutical Technical Transfer With Advanced Analytics 1/27/2021

    Improve pharmaceutical technical transfer and accelerate product approval.