“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.”

"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 …

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

"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. …

“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.”

"Castor’s all-in-one platform was a game-changer. One coordinator runs our entire study, saving us an estimated $100K in staffing while maintaining realtime data oversight. We’ve had nearcomplete questionnaire data, and the professional services team has been there every step of the way."

“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.”

"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."

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

"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."

"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."