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Do you comply with (clinical) regulations so I can run my CTIMPs (Clinical Trials of Investigational Medicinal Products) in Castor EDC/CDMS?

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There are many CTIMPS trials running in Castor EDC/CDMS. Castor EDC/CDMS complies with all applicable medical data privacy laws and regulations: Good Clinical Practice (GCP), 21 CFR Part 11, EU Annex 11, and the European Data Protection Directive. Using Castor EDC/CDMS, researchers can comply with all GCP guidelines applicable to them in their role as sponsor and/or researcher.

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  • Will my study be compliant with GCP (Good Clinical Practice) guidelines if I use Castor EDC/CDMS?
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