Catalent Clinical Supply Content

  1. Global Advantage With Free Trade Zones In China 7/14/2022

    Understand how free trade zones work, and explore a flexible and cost efficient way to supply clinical trials in China and around the globe.

  2. The Ultimate Guide To Clinical Supplies For Japan Studies 7/14/2022

    Our team in Japan provides comprehensive services including primary and secondary clinical packaging and labeling, comparator sourcing, cold chain storage, and local and global distribution.

  3. Overcoming Inventory Challenges For A Complex, Global Study 7/14/2022

    Explore how the optimization of Interactive Response Technologies (IRT) settings relieved the burden of managing global supply needs for a CRO customer and clinical sponsor.

  4. Specialized Expertise For Efficient Management Of Clinical Supply Budgets 7/13/2022

    A financial project analyst (FPA) plays a critical role in clinical trial supply and budget management. Explore how sponsors can benefit from having this specialist on their supply partner's team.

  5. Integrating Early-Phase Clinical Supply Manufacturing & Distribution 5/10/2022

    A tablet formulation was a solution when developing a new class of anti-infective medicine, allowing the integration of formulation development, clinical trial material (CTM) manufacturing, and supply and distribution to patients.

  6. How To Avoid Delays In Clinical Supply: Strategies For Comparator Sourcing 5/5/2022

    Learn about the ways in which sponsors can work effectively with clinical suppliers for accurate forecasting and comparator sourcing.

  7. Understanding Options In Direct-To-Patient Clinical Supply 5/5/2022

    Learn how DTP clinical supply enables participants to receive treatments in the convenience and comfort of their own homes while reducing (or eliminating) the need to travel to a clinical site.

  8. Accelerating Timelines By Planning For Clinical Supplies In Advance 7/21/2020

    Discover approaches in support of accelerated development timelines, including adopting a single vendor approach, engaging experts earlier in the development cycle, and performing timeline steps in parallel versus linearly.

  9. Navigating New EU Clinical Trials Regulation Requirements For Clinical Supplies

    Better understand Clinical Trials Regulation No. 536/201 (CTR) labeling changes and their potential to disrupt traditional clinical supply strategy that adhere to the new requirements.

  10. Optimizing Cell Therapy Supply Chains For Success

    When it comes to transporting highly sensitive and valuable materials, such as cell therapies, learn how teams can ensure that unique storage and distribution requirements are met.