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.

  Spring is in the air, the grass is getting green, and it’s the season for an invigorating change of pace. There’s no better time to look for new approaches to your programs, and of course a big part of that is exploring digital alternatives.

Implementing an electronic regulatory binder at your site may seem like a daunting task. Yet with increasing costs and excessive use of space associated with paper binders, the benefits of going paperless are undeniable.

Pharmaceutical sales representatives are generally over-burdened with programming options and responsibilities, and it can be difficult to sort through the noise and find truly impactful ways to connect with your target physicians.

Finding a good supplier match is a lot like dating. Don’t believe us? We’ve put together a list of what you should be looking for in a long-term vendor partner relationship.