Revolutionizing Drug Safety Report Distribution with TriPort Trial Portal: A Seamless Approach
In the fast-paced world of clinical trials, effective drug safety reporting is paramount. However,…
Decentralized Clinical Trials and Virtual Pharmaceutical Meetings
The pharmaceutical industry is continuing to evaluate and evolve the strategies and tools utilized…
The Necessity of a Virtual Attendance Option for Pharmaceutical Industry Meetings
The pharmaceutical industry continues to adapt to the evolving nature of virtual meetings and…
Four Tips to Engage Sites During Virtual Investigator Meetings
As clinical trials and training of sites become increasingly reliant on virtual technology,…
Best Practices for Pre-Meeting Planning to Ensure High Attendance
One of the most important aspects of live virtual events is the planning and organizing that leads…
Five Key Components For Remote Monitoring Solutions
Clinical trial monitoring is difficult and expensive, but key to a successful clinical trial. These…
Easy Clinical Trial Solutions to 4 Common Problems
New clinical trial solutions are changing the way we doing things for the better. Clinical research…
MedPoint Digital eISF Reference Model 2.0
The eISF Reference Model 2.0 brings new standards for eRegulatory and source document binders.…
InSite Virtual Monitoring: Reinventing the Remote Monitoring Visit
InSite Virtual is a powerful new digital solution for remote monitoring of investigator sites.…
Five Ways to Get the Most Out of eRegulatory and Source Document Binders
If you’re using eRegulatory and source document binders, these tips will take your team to the next…