Featured Articles

  1. How Paper And Electronic Source Data Meet ALCOA-C Principles 10/24/2022

    According to the Food and Drug Administration (FDA), data should meet certain fundamental elements of quality. If these best practices for source documentation aren’t followed, there is no valid evidence the test article is safe and effective. 

  2. Beginner's Guide To 21 CFR Part 11 Compliance 9/21/2022

    Computer systems used for clinical trials fall under Food and Drug Administration (FDA) 21 CFR Part 11. While Part 11 is widely known, this blog explains how it fits in with your research software.

  3. The Beginner's Guide To An Electronic Data Capture (EDC) System 7/20/2022

    In this blog, delve into a basic understanding of the EDC system and its role in clinical trials.

  4. 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.

  5. Effectively Working With A Research Technology Vendor During Implementation 12/22/2021

    In order to get the most out of your vendor partnership, here are steps to take when working with your vendor as you adopt and implement their technology for your organization.

  6. 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.

  7. 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.

  8. 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.

  9. 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).

  10. 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.