Featured Articles

  1. Prevent Patient Recruitment And Retention Issues With Digital Connections 9/16/2022

    This article covers  what the “patient experience” is in clinical trials, the problems with the patient experience in clinical trials, and four ways digital connections can create a positive patient experience in clinical trials.

  2. Too Many Trials, Too Few CRAs: Closing The Capacity Gap 9/16/2022

    The clinical trial industry has experienced 5.8% annual growth year over year–but the growth in CRAs and research sites isn’t keeping up. Read on to learn how these capacity gaps can be closed.

  3. How A Top 3 Global CRO Reduced The Impact Of CRA Hiring And Retention Challenges 8/22/2022

    Learn how a top 3 global CRO implemented technology to remotely connect with their research sites and can now monitor up to 50 sites per week, compared to the former average of two on-site monitoring visits per week.

  4. How To Reduce Operational Costs Of Clinical Trials In Uncertain Economic Conditions 8/22/2022

    In this article, discover how remote site collaboration platforms can help sponsors weather economic fluctuations when it comes to clinical trials.

  5. Technology Can Help Sites and Sponsors Prepare For The Upcoming Rapid Growth Of Clinical Trials 7/21/2022

    Delve into how repairing the broken links between sites, sponsors, and CROs can save the 22% of trials that fail due to lack of funding, resulting in hundreds of new treatments to patients faster.

  6. How eConsent Can Help Legally Authorized Representatives 6/22/2022

    Software vendors often forget to think about the needs of LARs, even though they play a vital role in clinical trials. Explore three ways eConsent can help LARs complete the informed consent process.

  7. FDA Guidance For Diversity In Clinical Trials: What You Need To Know 6/22/2022

    While diversity, equity, and inclusion have been major focuses for clinical research teams, sponsors and sites were excited to receive explicit FDA guidance in April 2022.  But what do clinical research teams need to know from the guidance, and how can they prepare to incorporate it?

  8. What You Should Know About ICH E8(R1) 5/18/2022

    As of April 2022, ICH E8(R1) is officially in effect. Since ICH E8(R1) revolves around study design, a deep understanding of the new guidelines to create study protocols is needed. Discover key takeaways for organizations that design protocols and run clinical trials. 

  9. How The New EU Clinical Trials Regulation Will Impact Sites And Sponsors And How You Can Prepare 4/25/2022

    The Clinical Trials Regulation (CTR) for the EU took effect on 31 January 2022. Sites and sponsors must now embrace the new regulations to successfully run clinical trials across the European Union. 

  10. Decentralization Of Clinical Trials Requires Digitization Of Clinical Trials – Is The Industry Wired For This Revolution? 3/21/2022

    Learn how the end result to decentralized trials is greater patient-centricity, higher enrollment, fewer drop-outs, and a faster study timeline.