Gathering and securing data throughout the lifecycle of a clinical trial is of utmost importance in order to preserve study integrity. To facilitate this collection of critical data, researchers need access to various case report forms. Luckily, many reputable institutions have created databases to address this specific need.
We’ve compiled a comprehensive list of reputable institutions and links to their study case report form documentation below. The resources are separated out by institution and include a brief summary of the case report form information you will find in each location.
A large amount of participant information is gathered at the initiation of a study; therefore organizations often identify efficiency bottlenecks during study startup. Study complexity has risen 325% over the past decade, but getting your study started fast contains more obstacles now than ever before.
As an added bonus to the case report form repository below, we want to help you in your efforts to reduce bottlenecks during study startup and throughout the lifecycle of your study. We’ve also assembled a kit of essential trial optimization resources to get you started:
- eClinical Solutions for Clinical Trials, for a complete outline of the top electronic solutions available for clinical trials.
- eISF Reference Model, so you know the industry’s current standard for setting up and managing an Electronic Investigator Site File.
- The Ultimate Guide to eRegulatory, a detailed guide to all things eReg and how choosing the right solution can accelerate study startup time and reduce costs.
We believe this kit will provide you with the knowledge and tools necessary to accelerate your studies!