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

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

"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."

"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.”

"As a startup, we are very data hungry. I love Castor and its tools - Being able to lock by participant and by field, using the tracking tool for snapshots of how we’re doing with enrollment, and the annotated CRF so sites can see what we’re looking for. We also …

"It’s easy and intuitive to build studies in Castor. The Castor Helpdesk with FAQs and the calculation tool were very helpful for study builds."

"I have to say that my experiences with Castor have been fantastic. It has been a really useful platform for us. The biggest advantage for us has been the facilitation of remote collaboration. We have had really good engagement with our studies, and I think it's just a very helpful …

“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.”

“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."

"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."

“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.”

“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."