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…

12 Best Practices for Virtual Meetings to Healthcare Professionals (Download Here) A Whitepaper by MedPoint Digital Virtual Meetings to Healthcare Professionals are very distinct from internal virtual meetings, requiring a different solution than self-service web conferencing. These external meetings often involve top-tier physicians who demand productive use of their time…

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…

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.

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.

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!

For any molecule or product, it is vital for pharmaceutical companies to gather important insights from key opinions leaders (KOLs) throughout the clinical development and marketing lifecycle.

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.