The Future of Pharmacovigilance Analytics and Insight
What will the next generation of reporting and analytics in ...
Real-World Data: From Dream to Reality
Concepts once thought to be theoretical are now a reality ...
5 Reasons to Move to Automated Safety Document Distribution
The very basis of pharmacovigilance is to detect, collect, monitor, ...
The Value of Interconnected Data Across the Drug Development Lifecycle
The management of data within organizations has far-reaching effects, as ...
Building an Open, Interconnected Regulatory Data Ecosystem
Most regulatory information management (RIM) systems were designed to capture ...
CTMS Solutions: Finding the Right Clinical Trial Management System
Managing a clinical trial is no small feat. Documents must ...
Benefits of a True SaaS Safety System
The Shift to the Cloud Historically, firms relied heavily on ...
3 Changes (and Benefits) of the EU Clinical Trials Regulation
The European Union (EU) Clinical Trials Regulation (CTR) harmonizes the ...
Best Practices in Safety Signal Analytics — Managing Today and Preparing for Tomorrow
With up to 30-50% annual growth in adverse event cases, how ...
How Leading South Korean Biopharma LSK is Modernizing Pharmacovigilance Operations with ArisGlobal
South Korean Contract Research Organization, LSK, spoke in a webinar ...
