MilliporeSigma Webinars

  1. Navigating Cleanroom Compliance For Safe Material Transfer 7/23/2024

    Watch to explore various aspects of environmental monitoring essential for the transfer of materials into controlled areas as well as recent advancements that can facilitate this task.

  2. How To Accelerate And Enhance ADC Therapies 6/24/2024

    Learn how payloads and advanced payload intermediates can expedite drug development and elevate ADC therapies, and explore ADC payloads, payload intermediates, and solubility-enhancing technology.

  3. Filling The Sterility Testing Gap: Traceability And 21 CFR Part 11 Compliance 6/6/2024

    Watch to learn about a solution that offers digital information for every stage of a sterility test while remaining compliant with 21 CFR Part 11.

  4. Overcoming Obstacles On The Journey To Commercialization 5/28/2024

    Explore case studies in the development and manufacturing of APIs and HPAPIs as well as innovative solutions designed to address and overcome challenges in bringing new medicines to patients.

  5. Strategic CMC Planning Through A Phase-Appropriate Quality Approach 5/28/2024

    A phase-appropriate quality approach ensures quality activities align with the unique risks and challenges of each development stage. Watch to learn how to apply such an approach to chemistry, manufacturing, and controls planning.

  6. Pressure Testing Your Readiness To Ensure GMP Batch #1 Success 5/28/2024

    Watch as an expert from an industry-leading CDMO provides insights into the crucial factors, challenges, and tech transfer methods needed to achieve right-first-time readiness and success.

  7. Building Better Degraders: Targeted Protein Degradation Partners 3/1/2024

    Learn from industry experts about the latest advances in chemical building blocks for protein degradation, including warheads, linkers, and ligands, and their role in constructing superior degrades.

  8. Considerations For Large-Scale API Production 3/1/2024

    Explore expert insights on selecting the right CDMO partner for large-scale API production as well as key considerations to ensure your small molecule API program is successful.

  9. PAT Implementation For ADC And Bioconjugation Processes 3/1/2024

    Explore expert insights into the implementation of Process Analytical Technology (PAT) for ADC and bioconjugation processes and the pros and cons of in(on)line testing for the conjugation process.

  10. Advancements In Process And Payload Development 2/29/2024

    Continuous advancements in the process and payload development of ADCs and next-generation bioconjugates have the potential to progress targeted therapeutics and improve patient treatment options.