CTMS Resources

  1. Come To The Dark (Mode) Side 3/7/2022

    Many of the decisions made by a product team start as suggestions from a user community of clinical professionals. While planning the development of a recently launched CTMS, a focus group was led where clinical professionals weighed in on potential improvements for a new system.

  2. eReg Benefits For Clinical Research: Use Cases For All Types Of Sites 5/1/2023

    Unearth the different kinds of eRegulatory use cases for diverse clinical site types and other eRegulatory capabilities designed to serve all sites.

  3. Build Versus Buy: What's The Best Tech Tool For Study Activation? 5/11/2023

    In the case of study activation, there are several compelling reasons that buying an appropriate purpose-built system is a better choice than taking on the challenge of building a study activation tool.

  4. Overcoming 5 Challenges Of Implementing eClinical Technologies 6/26/2023

    Assess five common pitfalls trial teams face when incorporating new technology and identify potential solutions to mitigate the common risks.

  5. The Future Of Clinical Trials Rests On A Unified CTMS Platform 8/1/2022

    Discover why a unified CTMS platform is the answer for managing both the clinical trial itself and the data it produces when it comes to poorly integrated clinical trial management systems (CTMS).

  6. Examining The "Why" And "How" Of Integrating Your eTMF And CTMS 6/24/2022

    As requirements for improved inspection readiness and quality risk management become more critical, discover the need to create a seamless integration and data flow between the eTMF and CTMS.

  7. HEOR In Action 5/14/2025

    Health Economics and Outcomes Research (HEOR) plays a vital role in guiding evidence-based decisions across the healthcare ecosystem.

  8. 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.

  9. Fujirebio Increases Study Agility By Streamlining Clinical Operations And Data Management Process 3/2/2022

    Fujirebio’s fast-growing U.S. Clinical R&D team was preparing for shorter studies with higher complexity. Traditional methods using paper and spreadsheet trackers were no longer adequate to meet quality goals. Learn how the group increased its agility and readiness with LifeSphere Clinical EDC and CTMS tools.

  10. A Few Clicks And Done: Automating EDC Data Entry 4/7/2024

    A novel solution has emerged to tackle the inefficiency and errors in manual data re-entry during clinical trials, streamlining data entry, eliminate application switching, and benefit all stakeholders.