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

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

"Castor’s all-in-one platform was a game-changer. One coordinator runs our entire study, saving us an estimated $100K in staffing while maintaining realtime data oversight. We’ve had nearcomplete questionnaire data, and the professional services team has been there every step of the way."

“Castor offers a truly seamless clinical trial experience for investigators and patients. Fast deployment was critical for us. Castor technology was easy to use and the self-service capability allowed us to deploy a study in just a few weeks.”

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

"User friendliness, affordable pricing and the flexibility of the Castor team made us choose Castor."

"What I like about Castor is that I can create a user-friendly database that will also create a user-friendly output, i.e. that I can already prepare the data as much as possible to make data analysis easier."

“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."

"Within 1 week, our students were comfortable using Castor and able to capture data."

"Building the case report form was quick and easy with the FormBuilder. We highly recommend Castor."

“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.”

“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.”

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

"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."