Patient Data Reporting White Papers & Articles

1. Consent By Proxy: The Key To More Inclusive, More Reliable Trials 4/17/2025

   Explore innovative digital workflow designed specifically for Legally Authorized Representative (LAR) to help overcome the challenges of complex documentation and data management issues.

2. Patient-Reported Outcome In Oncology Clinical Trials 4/17/2025

   As cancer therapies grow more complex and personalized, patient-reported outcomes (PROs) have emerged as a vital component of oncology research and care.

3. How Cloud ERP Overcomes Hidden Costs And Customization Constraints 4/17/2025

   Explore how Cloud ERP systems offer a transformative alternative, providing businesses with the flexibility to scale, adapt quickly to market changes, and benefit from seamless updates without extensive customization.

4. Taming The Complex Clinical-Trial Ecosystem 4/9/2025

   To navigate the growing number of vendor portals required for clinical trials, sites are seeking a vendor- and sponsor-agnostic solution to enable single sign-on and study organization.

5. Implementing An ERP System: 5 Key Steps To A Successful Rollout 4/3/2025

   Key success factors to implementing an ERP system include assembling a competent project team with leadership support, phased implementation to align with regulatory compliance, and careful data migration to ensure system reliability.

6. Why Legacy ERP Systems Are Draining Your IT Budget 4/3/2025

   Maintaining outdated ERP systems can consume up to 80% of an IT budget, leaving businesses stuck in a costly maintenance cycle that stifles innovation.

7. Feasibility/Site Selection Process Ripe For Improvement 4/1/2025

   One key to a more effective feasibility process is more transparent communications and collaboration between sponsors, CROs, and sites. Sponsors must provide clear information to each site to enable a more accurate recruitment assessment, and sites must properly digest the information to give an accurate projection. But how?

8. Why Empowering Sites Matters 3/27/2025

   The evolving landscape of clinical trials demands a site-centric approach to address the increasing complexities of patient recruitment, study start-up, and data management.

9. 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.

10. eTMFs Uncovered: 5 Costly Misconceptions To Avoid 3/21/2025

    Critically examine prevalent myths surrounding electronic Trial Master Files (eTMFs) and their integration with electronic Investigator Site Files (eISFs).