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
29.01.2025 22.01.2025	Implementation of the IVDR for CE Marking This course will tell about the IVD classification rules and the conformity assessment routes. Learn the importance of the...	Kursus	Regulatorisk Læs mere
07.02.2025 02.02.2025	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
03.03.2025 28.02.2025	MDR Auditing - Training of Internal Auditors in Relation to MDR Gain knowledge about the MDR requirements not covered by ISO 13485 and understand the MDR requirements related to the QMS...	Kursus	Regulatorisk Læs mere
04.03.2025 27.02.2025	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
24.03.2025 14.03.2025	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
30.04.2025 25.04.2025	Training of internal auditors in relation to country specific requirements within the MDSAP program The specific national requirements of the participating jurisdictions will be addressed with examples sampled over the...	Kursus	Regulatorisk Læs mere
24.06.2025 19.06.2025	Corrective & Preventive Actions (CAPA) This course is intended to familiarize participants with the requirements for a CAPA subsystem and the methods for effective...	Kursus	Regulatorisk Læs mere
22.09.2025 17.09.2025	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
01.10.2025 25.09.2025	Training of internal auditors in relation to country specific requirements within the MDSAP program The specific national requirements of the participating jurisdictions will be addressed with examples sampled over the...	Kursus	Regulatorisk Læs mere
27.10.2025 20.10.2025	MDR Auditing - Training of Internal Auditors in Relation to MDR Gain knowledge about the MDR requirements not covered by ISO 13485 and understand the MDR requirements related to the QMS...	Kursus	Regulatorisk Læs mere
10.12.2025 04.12.2025	Corrective & Preventive Actions (CAPA) - online This course is intended to familiarize participants with the requirements for a CAPA subsystem and the methods for effective...	Kursus	Regulatorisk Læs mere

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Online kurser

Online kurser

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