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Going Digital in Clinical Trials with Electronic Delegation of Authority, eSignatures, and Audit Trails
The adoption of digital solutions is becoming commonplace due to the increased efficiencies of electronic solutions in maintaining compliance in clinical trials. In this blog post, we’ll explore the critical components of going digital with
On-Demand Webinar: Mastering FDA Audit Readiness & Easing Site Burden
https://vimeo.com/898629213?share=copy Webinar Date: October 25, 2023 Discover the keys to audit readiness in webinar, “Mastering FDA Audit Preparedness: Streamlining Compliance and Easing Site Burden.” Our panel of experts unpack the potential of eRegulatory solutions in
On-Demand Webinar: A Journey Through eRegulatory
https://go.realtime-ctms.com/journey-through-ereg
How To Achieve a “No Findings” FDA Inspection Utilizing Remote Site Access
https://go.realtime-ctms.com/tekton-research
Top 5 Requirements for an Effective eReg/eISF Clinical Trial Solution
https://go.realtime-ctms.com/top-5-requirements
2020 Centerwatch Survey: Sponsors Place More Burden on Sites
https://go.realtime-ctms.com/centerwatch-survey
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