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
08.12.2023 01.12.2023	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
18.12.2023 11.12.2023	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
15.01.2024 08.01.2024	IVDD to IVDR Transition This course will tell about the key changes to requirements for CE marking following the publication of the new IVD...	Kursus	Regulatorisk Læs mere
29.01.2024 22.01.2024	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
29.01.2024 22.01.2024	Implementation of the MDR for CE Marking This course aims to offer guidance on implementation of the requirements stipulated in the MDR.	Kursus	Regulatorisk Læs mere
02.02.2024 27.01.2024	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
04.03.2024 27.02.2024	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
05.03.2024 27.02.2024	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
22.03.2024 15.03.2024	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
26.04.2024 19.04.2024	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
14.06.2024 06.06.2024	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
13.09.2024 06.09.2024	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
02.10.2024 27.09.2024	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
28.10.2024 21.10.2024	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
06.12.2024 30.11.2024	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

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