CTMS Resources

  1. Accelerating Your New Therapies Path To Market With Automation 10/1/2024

    Automation has become an essential tool for addressing the inefficiencies in traditional clinical trial methodologies, enabling trial teams to instead concentrate on critical tasks such as patient care.

  2. The Impact Of Automation In The Monitoring And Reporting Process 5/21/2024

    As clinical trial costs rise and ROIs decline, research teams are turning to automation to streamline monitoring and reporting processes without compromising data quality or regulatory compliance.

     

  3. 4 Questions To Ask CTMS Vendors 10/15/2021

    Here are four questions to ask during the vendor selection process to offer more insight into your future success with the selected vendor.

  4. Overcoming The Top 3 Challenges In Setting Up And Managing Clinical Trials 5/21/2024

    Navigating the intricacies of clinical trials demands adept handling of document management, regulatory compliance, and financial forecasting. Learn key strategies for overcoming these hurdles.

  5. Simplifying The Regulatory Submission Process With A Modern CTMS 12/14/2022

    Working in collaboration with industry representatives, explore the value that pulling the regulatory submission process into a modern Clinical Trial Management System (CTMS) could have.

  6. CTMS & Study Data: 2 Keys To Creating Optimal Process Transparency 5/8/2023

    Clinical trial management systems can either make or break operational workflows in medical studies. Listen to this discussion with Hope Weisser, Sr. Product Manager at TransPerfect, about the new features of Trial Interactive’s CTMS.

  7. De-Risking Clinical Trials: How A CTMS Can Help Adopt The ICH E6(R2) 6/20/2022

    Explore how CTMS capabilities can help uncover hidden study risks with industry-standard questions in the CTMS library, score study risk based on likelihood, impact, and detectability, and manage key risk indicators.

  8. The ROI Of eRegulatory And eIRB Integration 6/28/2022

    This article outlines common eReg management system integrations, and highlights a new integration already allowing sites to save hundreds or thousands of dollars per protocol.

  9. Flexible Integrations To Reduce Risks And Increase Efficiencies 10/4/2024

    Learn how a trial team kept the blind of central lab samples and patient treatment across a Phase III and extension trial, whilst optimizing the supply chain.

  10. The Evolution Of Technology For Safety Notifications 3/6/2025

    Discover how a digital-first approach empowers sponsors to optimize safety management and drive operational efficiency in an increasingly complex, global clinical landscape.