Clinical Trial Patient Technology Articles

  1. Penetration Testing In Healthcare: Common Vulnerabilities And Programs To Address Them 10/28/2025

    Explore some of the common pitfalls witnessed in healthcare environments, as well as guidance for implementing a penetration testing program. 

  2. Penetration Testing In Healthcare: HIPAA And GDPR Requirements 10/27/2025

    Learn about penetration testing requirements in the healthcare environment, including clinical research, according to HIPAA and GDPR. 

  3. What Sites Wish Tech Vendors (And Sponsors) Heard At SCDM But Probably Didn't 10/8/2025

    During a Society for Clinical Data Management (SCDM) panel discussion, three site-side representatives discussed the challenges clinical research coordinators have executing their clinical duties amid increasingly complex data entry demands.

  4. SCDM 2025: Practical Advice From Global Regulators — Including The FDA 10/6/2025

    Discover what regulators from around the world, including the FDA, think should be top of mind for clinical data managers.

  5. How To Pick The Perfect ePRO/eCOA For Your Trial (And Everyone In It) 9/8/2025

    Choosing the right ePRO/eCOA platform isn’t about comparing feature lists. It’s about asking: Will this work for patients, for sites, and for the trial as a whole?

  6. Ask An Expert Before Shredding Your Mobile Device CAPEX 8/14/2025

    Tasked with buying your company's mobile devices and not sure where to start? Discover the questions you should ask and the information you need to know before consulting an expert.

  7. Paving The Way For Sites To Use Their Own Tech 7/17/2025

    The DTRA has released a detailed playbook to help clinical research sites use their own validated technology in sponsor-led trials. The "Bring Your Own Technology" (BYOT) model aims to reduce tech overload at sites, improve efficiency, and preserve regulatory compliance — starting with eConsent as its first use case.

  8. eClinical Solutions Market To Double In 5 Years, As Sponsors Prioritize Efficiency 4/4/2025

    The global eClinical solutions market is projected to reach $22.1 billion in 2029, double its presence in 2024. Experts discuss the specific solutions driving market growth and share how they impact clinical operations.

  9. Is Double Programming Really Required For Validation? 3/10/2025

    Double programming has been the gold standard for validation, but technological advancements and improved sponsor oversight of CRO deliverables have introduced more efficient and reliable alternatives.

  10. Bring-Your-Own-Device For eCOA — Is It Worth It? 2/19/2025

    At the recent SCOPE Summit, four experts in data management, monitoring, site operations, and tech weighed the pros and cons of adopting bring-your-own-device (BYOD) requirements for clinical trial eCOAs.