White Papers

  1. Ready-To-Use Cartridges: Ensuring Compatibility For GLP-1-Based Drugs 8/27/2024

    Ready-to-use cartridges for GLP-1 applications offer safe, reliable self-administration. Discover how they can minimize complexities and better align with the stringent demands of modern pharmaceutical manufacturing.

  2. Design Testing Strategies To Develop A Drug-Device Combination Product 8/27/2024

    Leveraging the expertise and experience of a trusted partner can reduce risk and accelerate the time to market for drug-device combination products by creating an optimal Validation Master Plan.

  3. Solving The Silicone Challenge In Pre-Fillable Syringes 8/27/2024

    Discover a technology platform that is revolutionizing the pre-fillable syringe market by solving the challenge of silicone sensitivity, ensuring stability for sensitive drugs.

  4. Outsourcing Stability Storage: A Cost-Effective And Quality-Driven Approach 8/22/2024

    Partnering with a leader in outsourced stability storage is revolutionizing the pharmaceutical and medical device industry by saving costs and resources, and ensuring product quality and compliance.

  5. Nitrosamine Analysis: Solutions For Risk Management And Analytical Testing 8/22/2024

    Testing for nitrosamines is essential in the development and manufacturing of Active Pharmaceutical Ingredients (APIs) and drug products to ensure safety and compliance.

  6. The Benefits Of Incorporating Lean Methodologies Into Project Management 8/20/2024

    Delve into the core principles of lean project management and explore how these principles can be integrated with traditional methods to enhance project outcomes.

  7. Improving The Efficiency Of PFAS And Other High-Profile Analysis 8/12/2024

    Explore the advantages of Liquid Chromatography-Mass Spectrometry system monitoring software in PFAS analysis, including improvements in resource efficiency and operational performance.

  8. Improving Gene Therapy Development With Organ-On-A-Chip Technology 8/7/2024

    Explore the current challenges of developing gene therapies, the potential of Organ-on-a-Chip technology, the future of gene therapy, and more.

  9. From CLD To CDMO: Demonstrating A Successful Cell Line Technology Transfer 8/5/2024

    Explore critical considerations for biopharmaceutical developers and CDMOs during technology transfer as well as a successful transfer and scale-up of a cell line from a CLD platform to a global CDMO.

  10. Quality By Design: The Importance Of Reference Standards In Drug Development 8/1/2024

    Learn more about the comprehensive lifecycle management of reference standards, encompassing qualification, characterization, and storage procedures.