FEATURED ARTICLES

• Five Steps To User Adoption Of eRegulatory In Clinical Trials

  Gain insight from this collection of best practices when transitioning from traditional paper and fragmented technology workflows to a fully electronic and purpose-built eRegulatory platform.

• Clinical Trial Technology Report Showcases 2023 Trends: Site Enablement, eISFs, And Integrations

  Dive into six insights to stay on top of the rapidly shifting research industry and to ensure your research organization doesn’t get left behind. 

• How To Engage Frontier Sites Without Sacrificing Compliance Or Data Integrity

  By partnering with frontier sites, discover how sponsors and coordinating centers can make their trials more accessible and patient-centric.

• EU Annex 11: How To Stay Compliant

  EU Annex 11 lays out the European Union’s regulations for using computerized systems during clinical trials. Explore how sponsors and sites, who want their new medical treatment approved in the EU, must follow Annex 11. 

• How Global Regulations Impact Technology: Shared Responsibility For Maintaining Compliance

  When searching for clinical trial software, every site, sponsor and CRO has the same question: “how does this software comply with (insert clinical trial regulation here)?”  Learn the answers in this article.

• How Sites And Sponsors Can Collaborate For A Smooth Site Feasibility Process

  This article breaks down what sites and sponsors need from site feasibility and how a unified site-sponsor platform can address these needs and improve collaboration. 

• Prevent Patient Recruitment And Retention Issues With Digital Connections

  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.

• Too Many Trials, Too Few CRAs: Closing the Capacity Gap

  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. How can we close these capacity gaps, when most sites already have more trials than they can handle and there are ongoing CRA shortages? We must innovate.

• How A Top 3 Global CRO Reduced The Impact Of CRA Hiring And Retention Challenges

  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.

• How To Reduce Operational Costs Of Clinical Trials In Uncertain Economic Conditions

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

• Technology Can Help Sites and Sponsors Prepare For The Upcoming Rapid Growth Of Clinical Trials

  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.

• How eConsent Can Help Legally Authorized Representatives In Clinical Trials

  In this article, explore the three ways eConsent can help a legally authorized representative (LARs).

• FDA Guidance For Diversity In Clinical Trials: What You Need To Know

  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?

• What You Should Know About ICH E8(R1)

  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. 

• How The New EU Clinical Trials Regulation Will Impact Sites And Sponsors And How You Can Prepare

  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. 

• Decentralization Of Clinical Trials Requires Digitization Of Clinical Trials – Is The Industry Wired For This Revolution?

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

• Using Change Management For Digital Transformations In Clinical Trials

  Once you’ve implemented a new software or process into your clinical trial organization, you may find yourself asking, “Now what?” The answer to that is simple: focus on change management. 

• Study Start-Up Checklist For Digital Clinical Trials

  Read how five Florence employees with clinical research backgrounds came together to craft a checklist designed to walk sites through the process of tech-enabled study start-up.  

• 7 Key Findings From The 2022 Clinical Trial Operations Technology Survey

  Discover 7 key trends in clinical operations technology that your clinical trial team needs to know about.

• Helping Your Research Site Go Paperless

  In the available article, read about the three common concerns about going paperless with clinical research.