Intuitive and secure software for clinical trials: from electronic data capture (EDC) with eCRFs (electronic case report forms) to ePRO/eCOA/eDiary. Compliant with GCP, FDA CFR part 11, GDPR (german: DSGVO), ISO 14155. Meets all requirements of FDA, BfArM, ethic committees, MDR, IVD-R, and notified bodies. All kinds of studies possible and validated: academic research, clinical research, studies for product registrations, PMCF studies, pharma trials. The modular system allows you to configure the software to your specific needs - you only pay what you need. Made in Germany!