“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.”

"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."

"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."

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

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

"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."

"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 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.”

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

"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."

“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.”

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

“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."