CRF version control

Register and save different designed eCRF versions that your study can have over time.

ShareCRF allows to audit the changes that have been made in the design of the data collection application itself, keeping a record of each version and the date in which it was put into production. We can at any time check the history of publications and see which version of the CRF was operational on any day of the study.

The service complies with the requirements of the FDA 21 CFR Part 11 and ICH GCP in everything related to clinical trials, allowing the highest quality and safety for your studies and clinical trials.