Online kurser

Medicoindustrien udbyder online kurser i partnerskab med WMDO – som er den ledende globale udbyder af online kurser indenfor medtech. Du vil finde et omfattende katalog med mere end 200 online kurser indenfor:

- Pre-clinical
- Clinical evaluation
- Regulatory affairs
- Quality assurance
- Health economics and reimbursement
- Combination products
- Start-ups & business ethics.

Se Medicoindustriens kurser her

Kontakt

Berit Munkebo

Udviklingschef

49184708

bm@medicoindustrien.dk

Startdato	Emne	Type	Arbejdsområde
13.06.2022 10.06.2022	MDSAP Fundamentals and Readiness Training You will increase your knowledge of the guidelines for conducting MDSAP regulatory audits and the skills needed within your...	Kursus	Regulatorisk Læs mere
16.06.2022 14.06.2022	IVDD to IVDR Transition BSI will tell about the key changes to requirements for CE marking following the publication of the new IVD Regulation (IVDR...	Kursus	Regulatorisk Læs mere
07.09.2022 05.09.2022	MDD to MDR Transition BSI will tell you about the key changes in the transition from MDD to the new MDR - you will learn to identify the next...	Kursus	Regulatorisk Læs mere
12.10.2022 10.10.2022	Implementation of the IVDR for CE Marking BSI will tell about the IVD classification rules and the conformity assessment routes. Learn the importance of the General...	Kursus	Regulatorisk Læs mere
12.10.2022 10.10.2022	Implementation of the MDR for CE Marking The course focus on enabling you to draw up a clear concept or project plan, and how to integrate the requirements into your...	Kursus	Regulatorisk Læs mere
22.11.2022 18.11.2022	Digital Marketing of Medical Devices Abroad: Sweden, Germany, and USA The purpose of this course is to provide you a high-level overview of relevant rules to consider when structuring a...	Kursus	Regulatorisk Læs mere
30.11.2022 28.11.2022	Digital Marketing of Medical Devices Abroad: Norway, United Kingdom and France The purpose of this course is to provide you a high-level overview of relevant rules to consider when structuring a...	Kursus	Regulatorisk Læs mere
06.12.2022 30.11.2022	ANSI/UL 2900 Cybersecurity Testing for Medical Device Manufacturers In this training program, we will describe and demonstrate the minimum set of cybersecurity testing activities recommended...	Kursus	Regulatorisk Læs mere
07.12.2022 05.12.2022	Technical Documentation for Medical Devices According to the MDR BSI will learn you how to create robust technical documentation to demonstrate compliance to the MDR and better understand...	Kursus	Regulatorisk Læs mere
08.12.2022 06.12.2022	IVDD to IVDR Transition BSI will tell about the key changes to requirements for CE marking following the publication of the new IVD Regulation (IVDR...	Kursus	Regulatorisk Læs mere

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Online kurser

Online kurser

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