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

bm@medicoindustrien.dks billede
Berit Munkebo
Udviklingschef
49184708
bm@medicoindustrien.dk
Startdatosorter faldende Emne Type Arbejdsområde
12.04.2021
07.04.2021
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
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21.04.2021
14.04.2021
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
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10.05.2021
03.05.2021
IEC 62304: Software Lifecycle
This training aims to bring a complete overview of the implementation of the IEC 62304 for the development of a software as...
Kursus
Regulatorisk
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26.05.2021
22.05.2021
Process Validation
Every company producing medical devices needs to understand how to practically accomplish process validation
Kursus
Innovation
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03.06.2021
27.05.2021
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
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08.06.2021
03.06.2021
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
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15.06.2021
08.06.2021
IEC 60601 - How to Apply Safety and Risk Management to Medical Electrical Equipment and Systems
How to apply safety and risk management to medical electrical equipment and systems
Kursus
Regulatorisk
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17.06.2021
14.06.2021
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
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22.06.2021
16.06.2021
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