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

"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."

"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."

“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.”

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

"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 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."

"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."

“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."

“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."