Articles, App Notes, Case Studies, & White Papers

  1. The Future Of Remote Patient Monitoring In Decentralized Clinical Trials 5/8/2025

    Remote Patient Monitoring (RPM) is not just an innovation—it's a catalyst redefining how clinical research is conducted in the digital age.

  2. The Catch-22 Of eConsent: A Missed Opportunity For Improved Trials 3/21/2025

    Drawing on evidence from scientific literature, we examine the pitfalls that have hindered its success and propose actionable solutions to unlock its true value in clinical research.

  3. Tackling Feasibility In Rare Disease Clinical Trials 1/13/2025

    Rare disease clinical trials face distinct challenges, but the right data strategy can offer a transformative approach to addressing complexities and enhancing enrollment.

  4. Analyzing The FDA's Approach To Diversity In Clinical Trials 1/31/2025

    Learn how utilizing diverse data resources and collaborating with stakeholders enables sponsors to foster a culture of inclusivity, meet regulatory requirements and ultimately advance medical science.

  5. Information Security Is Vital For Decentralized Trials 11/6/2023

    Information is the most important currency to any business in the modern, highly tech driven world, and as a currency we should treat it with the utmost respect to avoid it being stolen, forged or devalued just like the money in your pocket. Learn what is crucial for data protection when running DCTs.

  6. DTx Company Leverages Real-World Evidence Platform In Registry Study 8/19/2024

    Discover how Castor’s eClinical system enabled a groundbreaking study in behavioral disorder treatment to collect Real-World Evidence (RWE) to support product research and claims.

  7. eTMF Systems Tell Compelling Story Of COVID-19 Vaccines 3/7/2022

    The rapid development of Covid-19 vaccines may lead more drug developers to increase their speed and agility by adopting electronic Trial Master File (eTMF) systems. In the case of Covid-19 vaccines, discover how eTMF systems tell a dramatic tale.

  8. Regulatory Guidance For PRO Strategy In Oncology Trials 11/10/2023

    Kelly Dumais, Principal Scientific Advisor, and Jowita Marszewska, Scientific Advisor at Clario eCOA, delve into the specifics of how recent regulatory advancements are influencing PRO Strategy.

  9. How MAC Clinical Research Innovates With CDMS/EDC 12/27/2023

    Discover how a partnership with one of Europe’s largest contract research organizations exemplifies the crucial role that technology plays in the realm of clinical studies.

  10. Remote Clinical Trial Monitoring: CRA Success In An Era Of Autonomy 4/5/2023

    As organizations become more skillful in training and monitoring CRAs, the latter can be empowered with greater flexibility and freedom in scheduling and travel.