About
Regulatory support for medical devices and in-vitro diagnostics
Our consulting services and seminars support you as a newcomer, start-up, manufacturer, distributor or supplier!
en.co.tec CONSULTING: Regulatory affairs and quality management for medical devices and in-vitro diagnostics. Professional support for ISO 13485, MDSAP, audits, risk management, gap assessment MDR-IVDR, technical documentation and much more.
With us you get individual support and customized advice!
en.co.tec ACADEMY: Practice-oriented training for medical devices and in-vitro diagnostics: in-house and public - on-site and ONLINE! From individual seminars to our online courses: REGULATORY SPECIALIST and MEDICAL SOFTWARE SPECIALIST to MBA Health Tech Management. We are also happy to outsource your training activities. For beginners and advanced learners!
Services
Life SciencesDiagnostics and TherapyMedical EngineeringConsultancy