Nov 23, 2021
As the clinical research ecosystem becomes more site and patient centric, I was curious about what an ideal software stack looks like for clinical research sites.
It goes without saying you need a laptop and stable internet connection to do business in this day and age.
But what else do you need to keep yourself...
Aug 31, 2021
Dr. Bierer is the Director of the Regulatory Foundations, Ethics and the Law Program of the Harvard Clinical and Translational Science Center and the Director of Regulatory Policy, SMART IRB.
Previously she served as senior vice president, research, at the Brigham and Women’s Hospital for 11 years, and was the...
Jun 30, 2021
This podcast episode highlights the top reasons for patient recruitment failure in clinical trials from an investigator perspective.
The podcast episode will help you understand how Sponsor and CRO personnel including software vendors can best support investigators meet or exceed their patient recruitment.
The goal...
Jun 7, 2021
Clinical trials are conducted in compliance with regulations.
Simply stated, you need a clinical and regulatory strategy when it comes to conduct of clinical trials for medical devices.
As a clinical researcher, there have been times I’ve felt lost because I did not understand the regulatory framework.
To close this...
May 31, 2021
The pandemic has helped fast track the adoption of technology in clinical research.
This has been a much needed change and we’re headed in the right direction.
The change in turn has led to an increased focus on decentralized clinical trials (DCTs).
But what exactly is a DCT?
To learn more, I invited Derk Arts,...