Featured Articles

31. Demonstrating Technical Excellence In Contract Manufacturing 12/10/2024

    Tech Talks explore ADC development innovations, including integrated supply chains, seamless pilot-to-GMP scale-ups, and advanced process analytical technology (PAT).

32. 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.

33. Integrating Phase — Appropriate Quality Standards 12/9/2024

    Phase-specific quality standards in biopharmaceuticals ensure GMP compliance, and maintain data integrity. Experienced CDMOs help balance quality expectations with accelerated development timelines.

34. 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.

35. 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.

36. 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.

37. 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.

38. 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.

39. 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.

40. 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.