Removing the Pain Points from Overburdened Medical Affairs Teams

Today’s Medical Information (MI) and Medical Affairs professionals are juggling multiple challenges: they must adapt to decentralization, outsourcing and globalization while tackling the rise of digital platforms and other ongoing changes affecting the pharmaceutical...

Adverse Event Reporting Software Gets a New Friend: Mobile

Every one of us at some point will take a medication and likely suffer some sort of adverse reaction. However, while some of us will actually read the product label and identify the possible adverse reactions, only a handful of us will ever report our experiences to...

New Rules Challenging Data Privacy Retention Processes

Data privacy and data retention seem to become more complicated by the day in the realm of medical affairs and pharmacovigilance. I am beginning to think that there really is no solution. With the GDPR (General Data Protection Regulation) coming in 2018 followed by...

Tomorrow’s Medical Information Tools Today

We know from our customers that for many medical information teams, being tasked with meeting pharmacovigilance obligations ensuring global compliance, as well as providing up-to-date, consistent and accurate medical information globally, can be a daunting prospect....