"The Castor Team has a strong experience with both research and data management which is very valuable to us."

"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 …

“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.”

"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."

"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."

"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."

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

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

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

"The rapid, widespread enrollment is a testament to the commitment of the WHO and its partners and was enabled by a design that allowed, for each patient, the rapid collection, recording, and transmission of a small amount of high-information data."

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

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

“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.”