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
09.11.2020 04.11.2020	Process Validation Every company producing medical devices needs to understand how to practically accomplish process validation	Kursus	Innovation Læs mere
09.11.2020 05.11.2020	Clinical Evaluation for Medical Devices in Europe and International Approach Course targeted towards clinical project managers, clinical research associates and others working in the field of clinical...	Kursus	Innovation Læs mere
16.11.2020 11.11.2020	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 Læs mere
17.11.2020 11.11.2020	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
25.11.2020 19.11.2020	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
25.11.2020 20.11.2020	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
01.12.2020 26.11.2020	EN 60601-series - 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 Læs mere
03.12.2020 27.11.2020	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
03.12.2020 30.11.2020	Introduktion til udbudsloven Et kursus for dig der du brug for at få helt styr på udbudsreglerne og ønsker et overblik over, hvordan man skal bruge dem i...	Kursus	Afsætning Læs mere
07.12.2020 02.12.2020	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
10.12.2020 07.12.2020	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
14.12.2020 10.12.2020	FDA Regulation of Medical Devices: Recent FDA Guidance Documents It is essential to understand the laws, regulations, processes and guidance for medical devices in order to be successful in...	Kursus	Regulatorisk Læs mere
22.12.2020 16.12.2020	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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