Featured Articles

  1. ADC Tech Talks Contract Manufacturing 12/9/2024

    Experts share strategies to accelerate ADC development, including optimizing supply chains, seamless scale-up to GMP manufacturing, and leveraging process analytical technology.

  2. Integrating Phase-Appropriate Quality Standards 12/9/2024

    Incorporating phase-specific quality standards ensures GMP compliance. Collaborating with an experienced CDMO addresses late-stage quality needs and efficiently manages development timelines.

  3. Choose The Rapid Methods Package For Your CHO Bulk Harvest Testing 11/26/2024

    Expedite success and be first to market with the Rapid Methods Package for your CHO bulk harvest testing. Find out how you can achieve 60% faster bulk harvest release testing.

  4. How To Boost AAV Titer With Feed Supplementation In Both HEK293 And Sf-9 Platforms 11/25/2024

    Explore how optimizing post-transfection or post-infection feeding in HEK293 and Sf-9 cells significantly boosts AAV titers, enhancing production efficiency for gene therapy applications.

  5. Integrating CPV And APQR Data And Workflows To Reduce Redundant Activities 11/15/2024

    Experts in the pharmaceutical industry share insights on how to effectively implement a strong, integrated CPV and APQR framework. Watch now and learn how automation enhances efficiency.

  6. Integrated Approach In Managing CPV And APQR 11/12/2024

    Many companies continue to manually collect data. Utilizing digital technologies can greatly improve productivity and efficiency by enabling real-time monitoring and streamlining regulatory reporting.

  7. Development Strategies For Adenovirus-Based Gene Therapies 11/11/2024

    Scaling up viral vector production can be challenging, and ensuring consistent titers and activity requires careful optimization and technical expertise.

  8. The Key To Viral Vector Success 11/11/2024

    Establishing a robust and scalable viral vector process requires a multidisciplinary approach that incorporates expertise in foundational science, analytics, and biomanufacturing.

  9. Regulatory Considerations Including Extractables & Leachables For Single-Use Manufacturing 10/29/2024

    Watch to gain insights into regulatory guidance for single-use manufacturing and risk assessment strategies for single-use implementation.

  10. Evaluation Of Extractables And Physical Compatibility Of The Mobius® ADC Reactor Single-Use Components For ADC Manufacturing 10/29/2024

    Explore study results evaluating the physical compatibility of single-use components in the Mobius® ADC Reactor and the level of extractables when exposed to dimethyl sulfoxide and dimethyl acetamide.