"Right from the beginning, the Castor team was quick to respond to our questions. This meant we were able to quickly get into more details and start building a solution together."

"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."

"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 …

“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."

"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."

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

"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."

"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."

"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. …

“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."

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

“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.”