Blog Archives

How One Global Pharma Navigated Change Management to Leverage Automation and AI

In the ever-evolving pharmacovigilance landscape , embracing automation and AI has become a strategic necessity for global pharmaceutical companies.

Why cloud is the only modern option for efficient, high-volume Safety data processing

Sam Wallis, Head of ICSR Case Processing within the Worldwide Patient Safety Operations at Bristol Myers Squibb, will join a Breakthrough 2024 panel discussion on the reality of transitioning Safety/Regulatory systems to the cloud. Here, he provides a glimpse into BMS’s own journey, which he’ll share candidly during the Day 1 debate.

Why Now Is the Right Time to Invest in Your First Drug Safety System

Small and emerging biopharma like yours face a crucial question ...

What is Regulatory Information Management (RIM)?

Regulatory Information Management (RIM) refers to an organization or team’s ...

While “Speed of Delivery” Tops the List of Medical Affairs Challenges, Active Use of Automation Is Still in the Early Stages

On June 18th, 2019, ArisGlobal presented the webinar “Effective Automated Content Management Strategies for Today’s Successful Medical Information Managers.” When polled, 40% of attendees rated “speed of delivering information” as their top challenge, yet only 13% have adopted automated component authoring to help remedy the situation. That and other interesting insights are shared in this first of a two-part blog series.