Remotely Manage Document Workflows with SiteLink
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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).
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Explore how technology can make study start-up more efficient and compliant for sites.
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Use this checklist to evaluate electronic consent solutions and determine what you need to ask vendors to reach your goals.
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Learn about the latest trends in digital research technology from our 2021 mid-year report.
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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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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.
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Over 400 pages answering 150+ questions sites have asked the FDA about using eRegulatory and eSource in clinical research.
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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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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.
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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.
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Learn how sites and sponsors can plan their technology strategies today for the clinical trials of tomorrow.
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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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