Articles, App Notes, Case Studies, & White Papers

  1. Rare Diseases And The Integrated CDMO Support System 4/7/2026

    Champion the rare‑disease community by advancing development models built on precision, continuity and global coordination that ensure every dose reaches the patients who need it most.

  2. FastChain®: A Solution For Made-To-Order Gene Replacement Therapy Study 3/12/2026

    Adopt a demand-led clinical supply strategy to reduce waste, optimize limited product supply, and accelerate patient access across global clinical trials.

  3. Transforming The Pharma Supply Chain 7/17/2023

    Start leveraging logistics partners with global end-to-end solutions that can help avoid costly delays, ensure high product quality, and accelerate impactful solutions for patients worldwide.

  4. Choosing RTSM? Evaluate The Team Running It, Not Just The Software 2/25/2026

    High-performing RTSM requires more than just code. Discover why team continuity and clinical expertise are the most overlooked factors in reducing trial risk and ensuring regulatory compliance.

  5. How Long Is Your RTSM Risk Mitigation List? 11/21/2024

    While RTSM systems help reduce many of the risks in clinical trials, each trial’s unique setup necessitates a risk analysis to identify trial-specific challenges.

  6. Enhancing Clinical Supply Chain With Signant SmartSignals Supplies 8/16/2024

    A global pharma leader improved supply chain efficiency and compliance by digitalizing processes with Signant's SmartSignals Supplies, achieving better visibility, traceability, and reduced errors.

  7. The Critical Role Of Clinical Trial Packaging Services In Trial Success 1/26/2026

    Compliant, accurate packaging protects product integrity, supports dosing consistency, and keeps studies running smoothly. Smart components and controlled processes lower risk across complex trials.

  8. Case Management Accelerates Shipment For SCN1A+ Dravet Syndrome Gene Therapy 3/12/2026

    Consider this streamlined, end-to-end solution that helped safeguard study timelines and ensured that patients with urgent medical needs could receive treatment without delay.

  9. Key Considerations For Labeling Your Cell Or Gene Therapy

    As sponsors focus on maintaining the temperature range required for cell and gene therapies, they must also keep in mind the challenges this task presents when properly labeling them for clinical trial distribution.

  10. Using IRT Data To Automate And Optimize Clinical Supply 4/17/2023

    Learn how clinical teams can save between $150,000 and $1 million in annual drug and shipping costs through automated supply optimization.