Featured Articles

  1. PUPSIT As Part Of A Contamination Control Strategy (CCS) 8/21/2024

    Learn about the changes introduced in the latest revision to EU GMP Annex 1, and gain insight into the components that should be part of a PUPSIT risk assessment.

  2. When Should Filter Validation Be Performed? 8/21/2024

    Learn about a program that has been developed to facilitate risk mitigation before process-specific filter validation is performed.

  3. The Scalability Of Depth Filters For CHO Cell Culture Clarification 7/19/2024

    Clarification using depth filtration is standard in monoclonal antibody (mAb) manufacturing. Here, we showcase the scalability of Stax™ mAx depth filters, demonstrating their effectiveness.

  4. Is Industry Ready To Take A Bite Out Of Obesity? 7/15/2024

    What are the clinical, economic, and policy considerations for a class of drugs offering a promising treatment for obesity, and how is the industry adapting to meet demand?

  5. New And Upcoming Trends In Immunodiagnostics 7/15/2024

    Explore the latest trends and cutting-edge technologies in immunodiagnostics that are transforming disease detection.

  6. CAR T Set The Pace So All Can Win The Cell Therapy Race 7/15/2024

    Gain insight into the modest origins of cell therapy manufacturing and how this history has paved the way for future advancements from Bill Shingleton, R&D Leader at Cytiva.

  7. When Measuring Filter Performance, Is Performance Absolute? 7/3/2024

    See why high-performing filters are inadequate for critical filtration processes and why sterilizing-grade filters are necessary to effectively remove undesirable species, including bacteria and viruses.

  8. Filtration Methods To Overcome New Challenges In Viral Safety 7/3/2024

    This study offers valuable insights to guide informed decisions in virus filtration, aligning with both the PDA TR-41 (2022) and ICH-Q5A guidelines.

  9. Optimizing Virus Filtration Validation 7/3/2024

    Explore guidance regarding the effective validation of a virus filtration process in the laboratory, including the fundamentals of viral filtration and an examination of relevant regulatory guidelines.

  10. A Sustainable, Efficient Approach To Enhance Equipment Qualification 7/3/2024

    Explore compelling reasons to digitize your qualification documents and the benefits of a sustainable and efficient approach that utilizes digital tools to enhance your equipment qualification process.