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

"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’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."

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

"Castor meets all our requirements GCP compliant, user-friendly, time-saver, audit trail."

"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."

“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 …

"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."

"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."

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

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

"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."