Life Science Webinars

  1. Become A REBEL With Your Cell Media Analytics 4/29/2021

    Watch this on-demand webinar to learn about technological breakthroughs that now allow for rapid at-line analysis of cell media. You’ll learn the fundamentals about this new technology, how and why to track key nutrients in your bioreactor, how to adjust your feed strategy based on rapid insights, and how to monitor consumption trends to drive high productivity.

  2. 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.

  3. Gene Therapy Downstream Manufacturing, Scale-up And Best Practices 4/5/2021

    Join our panel webinar and meet the authors of the recently published gene therapy Ebook: ‘Insights on Successful Gene Therapy Manufacturing and Commercialization’ downstream article.  Hear directly from the authors on various topics related to gene therapy manufacturing and commercialization, the current state of the industry and how we can continue to advance these life-changing medicines.

  4. Gene Therapy Upstream Manufacturing, Scale-up And Best Practices 3/31/2021

    Gene therapies provide innovative options for treating patients, particularly where other traditional therapeutics have been ineffective. The industry continues to grow and mature from research to approved therapeutics. In this panel webinar series, hear directly from the authors of the eBook  "Insights on Successful Gene Therapy Manufacturing and Commercialization" on various topics related to gene therapy manufacturing and commercialization, the current state of the industry and how we can continue to advance these life-changing medicines.

  5. Freezing Biologics For Storage And Transport 3/29/2021

    The process of freezing biologics for storage and transport is expected to play an increasingly important role in optimizing the supply chain as markets and production sites become more diverse. As the chosen freezing method can affect both product quality and amount of product loss, it is important to fully understand this critical step in the process. In this video we discuss an end-to-end solution to fill, freeze, transport and thaw bulk drug substances.

  6. General Scale-Up Strategies: Commonalities Between Mammalian And Microbial Processes 3/29/2021

    This webinar offers a general understanding of the concepts and tools required to successfully scale a process from bench to manufacturing. Focuses include the equipment adaptations required for execution of upstream and downstream processes at the manufacturing scale and common parameters used for organism growth and protein purification with a focus on mixing/agitation, gas flow, chromatography and filtration scaling.

  7. Implementing Single-Use Technologies In Formulation And Filling Of Vaccines 3/25/2021

    Formulation and filling is a critical part of any drug manufacturing process and demands the highest levels of quality and reliability. Pall has a range of technologies and services that enables end users to carry out their operations with increased reliability and flexibility – while ensuring the product quality is designed into the manufacturing process. Using technology from the Allegro™ single-use portfolio, Pall sterilizing grade filters and Pall’s automated solutions ensure that manual interventions are minimized and increased sterility assurance is achieved.

  8. Downstream Process Development For Vaccine Manufacturing 3/25/2021

    The purification of vaccines and gene therapy/viral vector products is a key part of a drug manufacturing process that requires high levels of product purity and process reproducibility. Pall has a range of technologies and offers field-based support and lab-based process development services that enable end users to purify and recover their high-value products. The process strategies to improve purity and yield as well as the challenges associated the purification of viral vector process will be discussed.

  9. Developing Scalable Upstream Workflows For Recombinant And Viral Vaccine Processes 3/25/2021

    Vaccine manufacturing is responding to challenges for increasing safety assurance and responsiveness in order to reduce the impact of pandemic such as SARS-CoV-2. Therefore, in-depth knowledge of microorganism pathogenicity leads to develop new type of vaccines such as recombinant and viral vaccines. In this presentation we will review the current main upstream vaccine production processes, considering the choice of expression system, the means by which the biological preparation is introduced into the production cell and how Pall’s flexible single-use bioreactors support rapid process development, scale-up and safeguard the quality of life-protecting vaccines and help assure compliance with cGMP.

  10. Vaccines Development, Regulations And Manufacturing Part-2 3/25/2021

    In Part 2, we will review vaccine processes with examples based upon influenza vaccine, inactivated Polio vaccine and an overview of the different types of vaccine production processes from cell expansion, USP and DSP, to the formulation and filling operations to make the finished product. We will talk about vaccine production facilities, how equipment is integrated their operating principles and biological safety levels for containment. Finally, we will look at the vaccine industry today, the supply chain and globalization, and how important vaccines are in pandemic preparedness, availability, and time to market.