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.

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!

Gathering resources for Case Report Forms is a great place to begin optimizing bottlenecks within your clinical trial operations. If you are looking to increase study start up timelines, decrease overall trial cost, and further reduce the time burden of manual processes, request access to our Clinical Trial Optimization Kit resources below.