Complete Guide to eRegulatory and eSource for Clinical Research
Check out this guide for an in-depth overview of how eRegulatory and eSource are impacting clinical trials and the steps you can take to prepare now.
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Featured Content
Resources built for clinical research professionals.
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Decentralized Clinical Trials for Research Sites
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Moving Beyond COVID – The Sponsor and CRO Perspective on Lessons Learned
Hear from top clinical operations leaders, from the world’s largest pharma companies to a company transforming how CROs operate, to learn how they adjusted their processes and technology post-COVID.
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How the Right Software Can Help Sites and Sponsors Navigate the FDA Approval Process
Sponsors, CROs, and research sites in the U.S. have always understood the importance of the FDA approval process. But with the arrival of COVID-19 vaccines, the general public has started paying...
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5 RFI Questions for Vendors Specializing in Remote Site Access Solutions
Many sites in the current pandemic landscape have limited or restricted on-site monitoring visits, increasing the demand for remote site access solutions across the industry. This shift is causing...
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The Complete Library of FDA eSource and eRegulatory Guidance
Over 400 pages answering 150+ questions sites have asked the FDA about using eRegulatory and eSource in clinical research.
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Diversity in Decentralized Clinical Trials | Why it’s Important and How to Improve
Many medical professionals worry about a lack of diversity in clinical trials, and this lack can have medical consequences. A 2014 study showed that around 20% of new drugs approved between 2008...
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9 Challenges and Risks for Launching Decentralized Trials
Decentralized clinical trials have exploded in popularity. A WCG survey showed that 94% of research sites have adopted at least one decentralized method, and 88% of sites have already hosted...
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Complete Guide to the Modern Electronic Trial Master File (eTMF)
We've gathered everything you need to know about choosing and implementing an eTMF into a single eBook. Download it before you choose an eTMF, or to get the most out of the eTMF you already have.
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Clinical Trial Technology Transformation: Creating an Effective Environment
The clinical research industry has historically been a laggard in technology adoption compared to other industries in healthcare. However, the COVID-19 pandemic lit the match, pressuring the...
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Building Clinical Trial Software Integrations Between Sites and Sponsors
As decentralized clinical trials become more popular, many sites and sponsors have begun to wonder how they can adopt decentralized methods without sacrificing compliance or efficiency. The...
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eRegulatory Evaluation and RFP Checklist
Use this checklist to avoid complications and headaches when implementing an eRegulatory solution by being equipped with the questions you should ask vendors.
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Five Ways Decentralized Trials Will Impact the Study Site
Decentralized trials will have a major impact on study sites and the clinical trial process. Some organizations refer to decentralized trials as “site-less” trials, but we disagree. As a clinical...
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Clinical Trial Sponsors and CROs Discuss Moving Beyond COVID
The COVID-19 pandemic created an unprecedented challenge across the clinical research industry. For sponsors and CROs, it meant developing a lifesaving vaccine and continuing ongoing clinical...
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2021 State of Clinical Trial Technology Industry Report
Hear the latest insights, trends, and analysis of how clinical trial operations are shifting heading into 2021.
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Everything You Need to Know for Remote Site Monitoring and Access
Everything You Need to Know to Prepare for Remote Site Monitoring and Access To keep your remote site monitoring plan from failing, study site acceptance must be your top priority when designing...
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How to Eliminate Clinical Trial Bottlenecks through Site Access
Sites, sponsors, and CROs now perform the bulk of their clinical trial operations by logging into cloud-based systems. The rapid shift to digital document and data management solutions opened the...
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Regulatory Compliance in the Global Clinical Research Evolution
Compliance Through the Lens of the Global Clinical Research Evolution The wheels of globalization have been turning at Florence for more than five years. As a purpose-built clinical trial...
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Key Benefits to a Modern eTMF
To evaluate the performance of your current eTMF system or of future vendors, download this guide to Key Benefits to a Modern eTMF.
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5 Steps to Activating Remote Site Access with Florence
You can enable remote site access for your clinical trial using these five steps.
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