Featured Articles

1. Early Product Characterization De-Risks Biologics Development 6/12/2019

   The relationship between physicochemical profile and biological activity — and how this relationship affects clinical performance — is key to informed decisions, accelerated development, and risk reduction.

2. Supporting Complex Manufacturing For Liquid And Lyophilized Drug Products 10/24/2025

   Aseptic fill and finish operations gain efficiency and precision with modular isolator technology, inline weight checks, and lyophilization, which are ideal for mRNA-LNPs and other sensitive modalities.

3. Cell Culture Media Filtration: Evaluating Cell Culture Performance 10/23/2025

   Cell culture performance remained consistent across PES and PVDF filters, even under worst-case filtration conditions. Discover a practical framework for evaluating membrane impact on CHO cell growth.

4. Key Factors In Selecting Your Ideal Microbial Air Sampler 10/7/2025

   Learn how to evaluate microbial air samplers based on collection efficiency and flow rate accuracy, as well as key factors that support data integrity and compliance in environmental monitoring programs.

5. Streamline Your AAV Process With A Production Platform 10/6/2025

   AAVs are reshaping gene therapy, but scaling production introduces complexity. Learn how upstream process optimization can improve yield, consistency, and speed to meet growing demands.

6. Achieve Higher Targeted Concentrations 9/30/2025

   Single-pass TFF streamlines downstream processing by reducing footprint, shear exposure, and hold-up volumes. Learn how this approach is advancing efficiency across therapeutic and vaccine production.

7. Effective Supply Chain And QC Testing Through Collaborative Partnerships 9/30/2025

   Explore how cross-functional teams streamline cell therapy manufacturing and release for Phase 1 trials to meet patient timelines and ensure safe delivery of personalized treatments.

8. Considerations In Sterility Testing And Assurance 9/23/2025

   Explore how sterility assurance, including sterilization validation and environmental monitoring, is essential for controlling microbial contamination in mammalian cell production to ensure patient safety.

9. Cell Culture Media Fingerprinting 9/8/2025

   Ensure consistency and quality in production with an advanced CCM fingerprinting technique that is capable of identifying over 100 media components to reduce variability and meet regulatory standards.

10. How To Fingerprint Cell Culture Media 9/8/2025

    Ensuring media identity and consistency is vital in biologics manufacturing. Discover why quantifying cell culture media components before batch release helps overcome formulation complexity.