Integration Update: Expanded FAQ for Advarra Merger Efforts
The Advarra team (formerly Chesapeake IRB and Schulman IRB) continues to integrate our processes and policies, leveraging mutual strengths in
The Advarra team (formerly Chesapeake IRB and Schulman IRB) continues to integrate our processes and policies, leveraging mutual strengths in
New to clinical research? Learn the meaning of common industry acronyms and abbreviations including eCRF, IIT, PI, TMF, and more.
Since November 2017, the Advarra team (formerly Chesapeake IRB and Schulman IRB) has been working to integrate our processes and
Learn the necessary steps to create an effective SOP for data collection in clinical trials.
On November 7, 2017, we announced that Chesapeake IRB and Schulman IRB are merging under the new organizational name, Advarra.
Learn the key characteristics that all NCI-designated cancer centers have in common.
Creating feasibility assessments can be as frustrating for sponsors as answering questionnaires is for sites. Here’s how sponsors can alleviate these frustrations, according to sites.
This post walks you through the basics of an electronic data capture system, providing a high-level overview of benefits and common functionality.
Wendy Tate, Director of Data Analytics at Forte, explains key skills and experiences sites look for in a clinical research coordinator.
Basics to help you get started measuring and improving your clinical trial performance.