"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."

"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."

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

"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."

"One of the many advantages of Castor is that they, as a company, are very innovative. Innovation is in their DNA, and this is a very good match with the dynamic world of medical research where we continually think of new functionalities and how to upgrade our surrounding ICT landscape. …

“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.”

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

“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."

"Castor has been a wonderful partner to work with. Their solution provides us with an integrated eConsent, ePRO, and EDC that's critical in our decentralized studies. The solution is backed by a fantastic support and technical team who's always willing to work with us to find solutions."

“It can be difficult to find fit-for-purpose trial solutions for studies that vary in size, complexity and face different budget constraints. We have partnered with Castor because their solution is easy-to-use and easily scales across varying regulatory environments.”

“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.”

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

"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."