The Impact of Remote Site Monitoring on Clinical Research Associates | Florence Benchmark Report 2022

A benchmark report of 143 global Clinical Research Associates (CRAs) who conduct remote monitoring through a digital link to the research site’s electronic Investigator Site File (eISF).

How Sponsors Can Reduce Chaos at Study Sites During Decentralized Trials

Study Start-Up Checklist for Digital Clinical Trials

Explore how technology can make study start-up more efficient and compliant for sites.

2022 State of Clinical Trial Operations Technology Report

Your Guide to Preparing an Annual Clinical Trial Site Budget

Florence eConsent Capability Evaluation Checklist

Use this checklist to evaluate electronic consent solutions and determine what you need to ask vendors to reach your goals.

Digital Research at Clinical Trial Sites: 2021 Mid-Year Survey Report

Learn about the latest trends in digital research technology from our 2021 mid-year report.

Decentralized Clinical Trials for Research Sites

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.

Understanding and Evaluating a Remote Site Access Solution for Monitoring and Source Data Verification in Clinical Trials

Remote site access is now a requirement for clinical trial operations. Review this checklist to help you successfully assess solutions and modernize your approach to monitoring.

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.

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.

Beginners Guide to Global Data Protection Regulation (GDPR) for Clinical Trials

Wondering how GDPR affects the clinical trial industry? Check out the tips for complying with GDPR that we've gathered based on our experience working with European clinical research sites.

Electronic Trial Master File (eTMF) Capability Checklist

Wondering which eTMF software has all the features you need to run successful clinical trials? Use this checklist to evaluate eTMFs and choose the one that's right for your team.

Complete Guide to eISF + Remote Site Access in Clinical Trials

Guide to Successful Change Management in Clinical Trials

Building the First Link in Decentralized Trials

Learn how sites and sponsors can plan their technology strategies today for the clinical trials of tomorrow.

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.

Proving The ROI of eRegulatory