Where Clinical Research Really Happens: The Investigator–Patient Visit
Clinical research programs span a massive array of contributing institutions, professionals, types…
Creating a Site-Centric Culture: The Key to Stronger Clinical Trial Partnerships
Global drug developers and investigators sites both recognize the value of being a good partner…
Winning the Competition for Patients
Leading pharmaceutical companies are expending more resources than ever to identify study subjects…
Transforming Clinical Research Processes with RASPberry AI
In the ever-evolving landscape of clinical research, the efficiency of Clinical Research Associates…
Strategies to Optimize Study Site Training Effectiveness
Avoid the Front-loaded Training Paradigm During the go-live period in a clinical trial, study…
Relieve your CRAs of the Site Training Burden
CRAs are tasked with an ever-increasing number of tasks and responsibilities to ensure that trials…
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…
BlogStudy Site PerformanceHCP Engagement
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,…
Launching a Strategic Virtual Advisory Board Partnership with a Leading Medical Communications Agency
Situation: In 2022, a large Medical Communications agency (MedComm A) approached MedPoint Digital…
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…