Your data is secure & your study compliant
Running a regulated trial has never been easier! Castor complies with all regulations such as HIPAA, 21 CFR Part 11, GDPR, GCP, and EU Annex 11. We are ISO 9001 and ISO 27001 certified. With our qualified team of experts, your study setup will be validated in days. We have a fully compliant package with all of the required documentation, and our team is ready to assist you during any audits. Read our case studies to learn more.Our security statement
Companies across the world trust us with their trial.
Made for commercial researchExplore our features
Decrease your time to market
Build your study within days, or have us build it for you, and be ready to start collecting data within weeks!
World class support included
We provide you with ongoing, world class support. Before, during and after your trial. Our support satisfaction is 96%.
Minimize your costs while maximizing the quality of your research, with Castor's transparent & competitive pricing.
View concise study statistics through clear dashboards. Let us create custom study reports to get real-time study specific insights that allow you to optimize your trial.
Integrate with your existing tools
Our API allows for seamless integration of Castor with you CTMS, IVRS or eTMF. Go for true eSource by connecting medical devices or wearables through our API or through our unique HL7 FHIR importer that streamlines clinical data reuse from any EHR system.
World class support
With our world-class support, your study will always be on track. Our customer success team answers your questions within the hour. Our support teams consists of highly knowledgeable technical, medical, and research graduates (CRAs).
Study building can be a time-consuming task. Save valuable time by having us build your study for you! As researchers, we have experience in building studies, and understand how to best set up your study within Castor. For customers who want extra support, we offer three packages: Two personal consultations, Pre-live check, and Phone support and priority email support. Contact us for a quote or for more information.
Full control over your study
You no longer have to rely on third parties to manage your study. With our flexible user rights management module, you can customize access for different users and user roles.
The investigator can easily see an overview of the study progress for his or her patients. Give your sponsor study overview and provide overview of all the queries, query statuses, and verifications to your monitor.
What our users say about Castor EDC.
Ariaan SiezenProject Leader Digital Research , Data Stewardship, Radboudumc
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 EDC is a really good partner to develop with.
PD Dr. med. Marco DüringPrincipal Investigator, Institute for Stroke and Dementia Research, LMU Munich
Castor strikes the right balance: Comprehensive features and easy to use at an affordable price.
Dr. Nienke LegdeurMD and Ph. D. Candidate at VU Medical Center
Within 1 week, our students were comfortable using Castor and able to capture data!
Paul TeunissenResearch Fellow, Department of Cardiology at VU University Medical Center Amsterdam
Building the case report form was quick and easy with the FormBuilder. We highly recommend Castor!
Jan de WaeleMD, PhD, Associate Professor at the University of Ghent
I find Castor EDC very easy to use! After watching the workshops I was able to easily create our eCRF in no time.
Josephine Lopes CardozoClinical Researcher, Amsterdam
Beautiful program that monitors your progress in data entry and quickly shows you if you have forgotten a step. Building the database was easier than expected and using Castor instead of Excel saved me a lot of time.
Jennifer BreelMPA Pain Medicine - Anesthesiology at the AMC
Castor meets all our requirements: GCP compliant, user-friendly, time-saver, audit trail.