Insights On Liquid Dose Manufacturing

1. Protecting Your Drug Product 5/13/2026

   With patient lives depending on every dose, even minor vulnerabilities in containment or delivery systems can have serious consequences for product integrity and patient outcomes.

2. 0.45 m/s ±20% At Working Position In Closed Sterility Testing Isolators: Requirement Or Convention? 2/19/2026

   Balance compliance and efficiency in sterility testing. Explore how a risk-based approach to airflow and isolator technology aligns with Annex 1 while optimizing contamination control.

3. Turnkey Dismantling, Modification, And Relocation Of A Multi-Glove Isolator System 1/30/2026

   Strategic equipment relocation and retrofitting can reduce capital costs by fifty percent and save months in lead time. Learn how to modernize legacy systems while maintaining full GMP compliance.

4. Seasonal Vaccine Manufacturing: 3 Areas To Evaluate When Selecting A Partner 10/16/2024

   Experienced outsourcing partners will have the right facility and technical capabilities, a culture of speed and execution, and shared expectations and commitment to continuous improvement.

5. Lyophilization To Enable Drug Products Containing Labile Molecules 6/6/2025

   Develop lyophilized formulations to overcome stability challenges and significantly extend the shelf life of sensitive therapeutic products.

6. CDMO Uses Robotic Gloveless Isolator For Advanced Therapeutics 4/28/2025

   CDMOs must innovate production architectures to meet the demands of advanced therapeutics to ensure a reliable supply and compliance. Discover how these approaches advance modern medicine and improve patient outcomes.

7. Ensuring Product Safety And Purity With Mycoplasma And Sterility Testing 10/7/2024

   Discover how the Applied Biosystems™ MycoSEQ™ Plus system and Applied Biosystems™ SteriSEQ™ Rapid Sterility Testing System can help accelerate your cell therapy manufacturing process.

8. Gain Speed To GMP Filling 2/24/2025

   Discover the advantages of a filling technology that provides faster readiness to good manufacturing practices (GMP) filling compared with traditional options.

9. Compressed Gas Systems In Aseptic Manufacturing 10/18/2024

   Learn about compressed gas systems and why effectively identifying and managing the risks associated with these systems is critical for maintaining product quality and ensuring compliance with GMP.

10. The Successful Implementation Of A New Aseptic Filling Line 10/10/2024

    Discover how a Quality by Design approach can streamline the development of new sterile product filling lines, featuring a real-life example illustrating its effectiveness.