MedPoint Digitial eISF Reference Model 1.0 (Click here to download) MedPoint Digital and MAGI announce with great enthusiasm that the MAGI Global eISF / eReg Binder Reference Model, Version 1.0 is now presented to the public. Filip Matakovic has been passionately involved as the MedPoint representative in the MAGI eISF…
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FarSite™ Virtual Visits: Bringing Patients and Investigators Closer Together
Virtual clinical trials can significantly reduce the need for patients to travel to sites, allowing many more patients per site to participate. This enrollment effect can lower the total number of sites required in a trial, leading to powerful cost reductions. Virtual trials also offer other advantages, such as improved…
Continue ReadingInSite Virtual® Monitoring: Reinventing the Study Site Visit
InSite Virtual® Monitoring is a powerful new digital solution for investigator site monitoring, employing innovative virtual technology so CRAs can perform core monitoring functions without travel. By eliminating the significant expense and downtime of travel, InSite has the potential to significantly lower costs of clinical trials.
Continue ReadingJoin MedPoint Digital on the Path to Paperless!
Are you feeling burdened by regulatory paperwork? Watch to learn more about RegDoc eSafe, a validated, 21 CFR Part 11 compliant eReg system that provides a paperless solution to several challenges facing clinical study sites.
Continue ReadingStudy Site Training: What Method is Best?
People often ask, what is the best way to train study sites for a clinical trial? At MedPoint Digital, we believe in an overarching approach that’s customized to fit the needs of individual studies. Watch to learn more!
Continue ReadingMedPoint Digital Welcomes Yvonne Reid
MedPoint Digital would like to extend a warm welcome to Yvonne Reid, the newest addition to our Global Development Team. Yvonne will be working from MedPoint Digital’s new West Coast Office. We are thrilled to have her on board! We sat down with Yvonne to learn more about her impressive…
Continue ReadingInSite Virtual® Monitoring: The New Option for Site Monitoring
The clinical research associate (CRA) plays a significant role in the life of a clinical trial, monitoring all activities to ensure compliance with the study protocol and ICH-GCP guidelines.
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