"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."

“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.”

"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."

"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."

"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. …

"Within 1 week, our students were comfortable using Castor and able to capture data."

"Building the case report form was quick and easy with the FormBuilder. We highly recommend Castor."

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

“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.”

"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."

“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.”

"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 …

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