Integration Update: Revised FAQ for Advarra Merger Efforts
Since November 2017, the Advarra team (formerly Chesapeake IRB and Schulman IRB) has been working to integrate our processes and
Technology
Data Collection in Clinical Trials: 4 Steps for Creating an SOP
Learn the necessary steps to create an effective SOP for data collection in clinical trials.
Schulman IRB and Chesapeake IRB Merger and Integration: What You Need to Know
On November 7, 2017, we announced that Chesapeake IRB and Schulman IRB are merging under the new organizational name, Advarra.
The Six Characteristics of an NCI-Designated Cancer Center
Learn the key characteristics that all NCI-designated cancer centers have in common.
6 Ways Sponsors Can Improve Feasibility Questionnaires
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.
Beginner’s Guide to an Electronic Data Capture (EDC) System
This post walks you through the basics of an electronic data capture system, providing a high-level overview of benefits and common functionality.
Deciphering the CRC Career Path: Key Skills and Responsibilities
Wendy Tate, Director of Data Analytics at Forte, explains key skills and experiences sites look for in a clinical research coordinator.
Beginner’s Guide to Clinical Trial Performance Metrics
Basics to help you get started measuring and improving your clinical trial performance.