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SIQ: Online course: Products Without an Intended Medical Purpose – Regulation (EU) 2017/745, ANNEX XVI 09:00
SIQ: Online course: Products Without an Intended Medical Purpose – Regulation (EU) 2017/745, ANNEX XVI @ ONLINE
Apr 24 um 09:00 – 12:15
SIQ: Online course: Products Without an Intended Medical Purpose – Regulation (EU) 2017/745, ANNEX XVI @ ONLINE
This workshop will be in English and is part of our new academy cooperation with the Slowenian notified body SIQ! What are products without an intended medical purpose? Contact lenses or other items intended to[...]
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START: Online-Course: MEDICAL SOFTWARE SPECIALIST 09:00
START: Online-Course: MEDICAL SOFTWARE SPECIALIST @ ONLINE
Apr 26 um 09:00 – Jun 7 um 16:30
Your career stepping stone into the world of medical software & apps! On April 26, 2024, our practice-oriented certificate course will start on all regulatory requirements for medical software and applications in a compact online[...]
Basic course: Development of software for medical devices 09:00
Basic course: Development of software for medical devices @ ONLINE
Apr 26 um 09:00 – 16:30
This seminar will be held in English. The development of standalone software such as mobile medical applications but also the integration of software as a component in medical devices means a complex challenge for many[...]
SIQ: Online course: Guidelines for Managing Medical Device Cybersecurity in Design, Installation, and Maintenance 09:00
SIQ: Online course: Guidelines for Managing Medical Device Cybersecurity in Design, Installation, and Maintenance @ ONLINE
Apr 26 um 09:00 – 15:00
SIQ: Online course: Guidelines for Managing Medical Device Cybersecurity in Design, Installation, and Maintenance @ ONLINE
This workshop will be in English and is part of our new academy cooperation with the Slowenian notified body SIQ! About the training This seminar takes a system approach to protecting medical devices, systems, networks,[...]
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  1. […] empfehlen wir Ihnen unsere Online-Seminare, unseren Online-Lehrgang: Regulatory Expert MDR / IVDR und NEU: MBA Health Tech […]

  2. […] dieser Woche starten wir mit neuen Basiskursen zu allen wichtigen Themen für Medizinprodukte- und In-vitro […]

  3. […] Wir empfehlen Ihnen, die verbleibende Zeit zu nützen und die Anforderungen an die UDI-Kennzeichnung Ihres Medizinprodukts bzw. In-vitro Diagnostikums umzusetzen. Dann sind Sie rechtzeitig fit für die Registrierung in EUDAMED! Hier geht’s zu unseren aktuellen UDI-Seminarterminen. […]

  4. […] Hier kommen Sie zu unseren Seminarterminen im Herbst! […]

  5. […] en.co.tec Akedemie veranstaltet am 16.Juni 2021 ein Seminar zum Thema: Medical Device Single Audit Programm (MDSAP) mit Mag. Thomas van den Oever. In diesem Seminar lernen Sie, das Audit-Modell richtig zu interpretieren und wissen, welche […]

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