Clinical Supply Regulatory Solutions

  1. Importer Of Record (IOR) Services For Clinical Trials 8/10/2026

    Global clinical trials face customs challenges. A synchronized Importer of Record service ensures compliance, streamlines logistics, and helps prevent shipment delays.

  2. The Future Of Glass Packaging Is Here

    Review the potential of Corning Valor® Glass to optimize the fill/finish process and reduce total cost of quality as well as overall manufacturing cost.

  3. Cell And Gene Solutions To Power Your Success 9/19/2023

    The number of CGTs advancing toward clinical trials and commercialization is increasing, making it crucial for sponsors to find innovative solutions and leverage industry expertise to maintain a competitive edge.

  4. Go Beyond Orchestration: Delivering Advanced Therapy Lifelines

    Advanced treatments such as cell and gene therapies require sophisticated logistics to ensure product quality and efficacy. Explore the comprehensive solutions to support your therapy product through clinical and commercial.

  5. Simplify Logistics With Total Transportation Management

    Advanced therapeutics and global patient population pools present unique logistical challenges, making it important to mitigate supply chain risk by simplifying the complexity associated with transportation planning and monitoring.

  6. Centralize Your Labeling Workflow Management 12/16/2022

    TransPerfect Life Sciences supports clinical supply teams with an end-to-end labeling process that ensures compliance and reduces timelines to speed up regulatory approvals.

  7. Scalable Manufacturing Of Sterile Drug Products 3/31/2023

    Discover comprehensive clinical to commercial scale manufacturing services that deliver true life-cycle management for sterile drug products that bring treatments to patients with efficiency and quality.

  8. Technology To Enable Remote Participation 12/15/2025

    Secure, flexible virtual visits boost trial efficiency and patient engagement. Global reach, device integration, and intuitive scheduling reduce disruptions while ensuring compliance and data security.

  9. What Does It Take To Guide A Combination Product Down The Path To Regulatory Submission?

    As one pharmaceutical company learned, it takes support from the right partner to create an on-body device that can safely and reliably deliver their medicine—while empowering patients to take control of their own health.

  10. Manufacturing Science & Technology (MS&T) And Supply Chain 4/27/2022

    At Kymanox, the Manufacturing Science & Technology (MS&T) and Supply Chain team, with its global experience in the biopharmaceutical and medical device industries, provides support for all product development phases from early clinical to post-commercial life cycle management.