GenAI’s large language models will transform safety & regulatory processes
Up to now, AI technology has had to be painstakingly ‘trained’ in what to look for.
Harnessing Medical Affairs’ Strategic Potential
When saddled with legacy medical information systems, Medical Affairs teams ...
Getting More Value from Your Data Through a Unified, Cross-Department Platform
At this year’s DIA Global Annual Conference, ArisGlobal presented an Innovation Theater session, “Getting More Value from Your Data Through a Unified, Cross-Department Platform.” Wim Cypers, Senior Vice President of Regulatory, highlighted use cases where automation can be used to improve business processes to enhance data quality and improved business process efficiencies.
Examining The Unified Future of Regulatory Platforms With Astellas
As the pharmaceutical industry adapts to a new world with ...
Experience, Expertise, and Understanding – Building Critical Insight into Smart ICSRs
Individual Case Safety Reports, or ICSRs, are a large part ...
From Push to Pull – Making the Triage of Adverse Events Downloaded from EMA Hassle Free
There has been significant changes in the way the EMA expects MAHs to handle ICSRs from the new EudraVigilance system, creating additional work for already busy pharmacovigilance departments
Embracing the Cloud: A Transformative Journey in Regulatory Operations
In the ever-evolving world of pharmaceuticals, a leading company has embarked on a transformative journey by moving its regulatory operations to the cloud.
Evolving Pharmacovigilance Beyond a Cost Center
Safety is evolving rapidly. There is a major, emerging opportunity ...
EMA SPOR Working group release the details to the SPOR Change Liaison Group
EMA SPOR Working group release the details to the SPOR ...
Enabling an Evidence-Based Approach to Pharmacovigilance and Safety
Safety departments at Marketing Authorization Holders & Regulatory Authorities are ...
