Featured Articles

31. A Beginner's Guide To Compliant Electronic Source Data Capture 10/15/2021

    With today’s complex trials, the expectation of gathering faster results in an increasingly decentralized environment is only increasing, imploring investigators to implement electronic source data capture systems. How can researchers ensure this is done correctly? Leveraging the right technology to standardize a compliant process for source data capture is a proven way to reach these goals.

32. 4 Key Integrations For Your Clinical Trial Management System 9/14/2021

    Discover how implementing a clinical trial management system (CTMS) can generate significant improvements to the way an organization understands their research portfolio, manages the financial components of trials, leverages reporting and analytics, and more.

33. Understanding eSource, ePRO, And EDC 9/14/2021

    As the clinical research industry becomes more technology-centric than ever before, it’s becoming more common to work with connected technology platforms to streamline studies. Read about working with integrated eSource, electronic patient-reported outcome (ePRO), and electronic data capture (EDC) systems.

34. Key CTMS Capabilities To Improve Financial Management 8/9/2021

    In clinical research, utilizing your clinical trial management system (CTMS) to its fullest potential can allow for more streamlined financial management, visit management, compliance, patient recruitment, and more. This blog outlines what you should look for in a CTMS to maximize your organization’s return on investment (ROI).

35. Site Technology Guide For Facilitating GCP In Decentralized Trials 8/9/2021

    Depending on the level of decentralization of your trial, you need secure cloud-based technology to adhere to Good Clinical Practices (GCP) while overseeing, communicating, and managing the entire trial process. Read how the best tools are scalable to any level of enterprise complexity and help maintain study quality, while allowing you to adapt to any level of decentralization according to protocol.

36. 12 Items Auditors Look For When Reviewing An Investigator Site File 7/22/2020

    Maintaining complete, compliant documentation on top of managing the complex processes and interactions of clinical trial conduct can be challenging. Explore twelve items to help you prepare your ISF for an audit.