Name: Complion integrates with WCG Connexus to automate clinical trial document flow
Uploaded: 2022-03-28T19:34:30.000Z
Duration: 1 min 59 s
Description: Complion integrates with WCG Connexus to automate clinical trial document flow

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The MasterControl Quality Excellence suite bundles a number of products supporting work quality and compliance including training and exams, incidents and corrective actions (CA), documents and change, and other modules.

MasterControl Quality Excellence

Complion eReg/eISF Platform

A Clinical Trial Management System(CTMS) supports research institutes and pharmaceutical to run clinical studies with human subjects. Therefore they store subject information and support research operations with planning, benchmarking, and reporting features, and also should integrate with a business intelligence or analytics platform, if it does not contain such features intrinsically.

Clinical Trial Management

Complion is a leading provider of eRegulatory and eISF solutions for Sites, Sponsors and CROs. Founded by a clinical researcher participating in an NIH-funded MD/PhD training program, Complion’s unique cloud-based purpose-built software enables collaboration of site regulatory workflows and the management of essential documents to ensure clinical trials are conducted in an audit-ready manner.

Complion, Inc

Complion integrates with WCG Connexus to automate clinical trial document flow

Complion accelerates site startup and closeout with eISF/eReg integration to WCG IRB Connexus and WCG Velos eResearch CTMS.   In this short overview, see how any site globally is a single click away from connecting Complion to all of their WCG IRB protocols on Connexus for efficiently managing their cIRB documentation electronically into their own eISF seamlessly.
Learn more:   https://complion.com/complion-now-connected-to-wcg/

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Complion eReg/eISF Platform

Overview

What is Complion eReg/eISF Platform?