“Thanks to Castor, we were able to easily integrate eConsent with ePRO, and EDC for our study needs; we believe Castor’s approach will help lead to trial success and account for patient adoption of our approach to decentralized clinical trials and Click Therapeutics study technology.”

“This this a great benefit as the budget of investigator initiated studies normally won’t allow extensive monitoring of entered data.”

"Castor allows us to be in control of our study and confidently run a study that follows good clinical practices, all at a fair price point."

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

"All things considered, it took me around 30 hours for the study build, whereas without Castor it would’ve probably taken more like 80."

"Castor strikes the right balance Comprehensive features and easy to use at an affordable price."

"From a research manager or a coordinator’s perspective, Castor’s platform saves a lot of time, approx. 1-2 hours a day, which is a huge benefit when you’re a part of a small research team."

"I’m not a PC whizz, but with your guidance I was able to quickly and easily build my CRF."

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

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

"Having an EDC system that can keep everything together is very important to successful research – especially when there are many variables like different languages, changes of shift, etc."

"Right from the beginning, the Castor team was quick to respond to our questions. This meant we were able to quickly get into more details and start building a solution together."

“Castor’s solutions were easy to navigate and intuitive to use, which is why we were interested in working with them. They were able to accommodate the amount of data from our multi-site randomized controlled trial, and our sites have expressed how much they have enjoyed using Castor as well.”

“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."