“I found it very easy to use! After watching the workshops I was able to easily create our eCRF in Castor.”

"Castor meets all our requirements GCP compliant, user-friendly, time-saver, audit trail."

"As a new user to Castor, the study build was quick. It took approximately one month with additional time for user acceptance testing."

“We knew that if we went with Castor, we would have the support we needed moving forward, and would be able to discuss future studies and develop the tool to meet the needs of both current and future projects."

“It was easy to create our clinical trial workflow. Integration and training with external partners was effortless. Usability and light coding were essential to us. We were able to test and build our own studies with minimal support and admin.”

"Taking the ‘perfect match’ into consideration, social media recruitment and pre-screening done by Link2Trials and Castor’s eConsent/eCRF tools helped to increase the rate by at least 2x. [It would have been] even higher if the site would have had the chance to manage all patients."