MedTech Academy

MedTech Academy courses provide a complete overview of all upcoming course dates within regulatory compliance, quality, software, biocompatibility, documentation and market access.

Emne

Aktivitetstype

Dato

Sprog

Søg Nulstil

7. September 2026

Person Responsible for Regulatory Compliance according to MDR and IVDR

9. September 2026

New Implementing Act, Annex VII: Time to Market - Predictability & Increased Transparency

17. September 2026

Workshop on clinical evaluations and investigations with medical devices

21. September 2026

Technical Documentation for Medical Devices According to the MDR

25. September 2026

Introduktion til UDI (Unique Device Identification) - Identifikation og mærkning af medicinsk udstyr

28. September 2026

Digital markedsføring af medicinsk udstyr

29. September 2026

US Quality Management System Regulation (QMSR) and other US Regulations for Medical Devices

1. October 2026

New update on China NMPA Regulation and Registration for Medical Devices

1. October 2026

IEC 60601 - How to Apply Safety and Risk Management to Medical Electrical Equipment and Systems

5. October 2026

IRCA Certified ISO 13485:2016 QMS Lead Auditor Training for Medical Devices

5. October 2026

Training of internal auditors in relation to country specific requirements within the MDSAP program

7. October 2026

Industrial Sterilization of Medical Devices - An Introduction to the Practical Approach of Sterilization

4. December 2026

Introduktion til udbudsloven

7. December 2026

Practical Leadership in Medtech – From Specialist to Impactful Leader

9. December 2026

Rules on Advertising, Affiliation, and Financial Benefits

10. December 2026

FDA Regulation of Medical Devices: Recent FDA Guidance Documents

14. December 2026

Reimbursement as a Driver for Commercial and Clinical Strategies

15. December 2026

Threat Modelling, Security Architecture and Controls for Medical Devices: Attacking and Defending

17. December 2026

IEC 62304: Software Lifecycle

21. December 2026

Corrective & Preventive Actions (CAPA)

18. January 2027

Introduction to the IVDR for CE Marking

22. January 2027

Introduktion til UDI (Unique Device Identification) - Identifikation og mærkning af medicinsk udstyr

28. January 2027

Introduction to MDR (2017/745)

1. February 2027

IEC 60601 - How to Apply Safety and Risk Management to Medical Electrical Equipment and Systems

4. February 2027

GAP between ISO 9001 and ISO 13485

22. February 2027

Person Responsible for Regulatory Compliance according to MDR and IVDR

25. February 2027

Combination Products - Regulatory & Quality Introduction

1. March 2027

Digital markedsføring af medicinsk udstyr

4. March 2027

MDR Auditing - Training of Internal Auditors in Relation to MDR

15. March 2027

Training of internal auditors in relation to country specific requirements within the MDSAP program

19. March 2027

Introduction to Chemical Compliance for Medical Devices

2. April 2027

Introduction to Polymer Materials in Medical Devices - from a Biocompatibility Risk Perspective

12. April 2027

Project Management for Product Development of Medical Devices

26. April 2027

AI in Medical Device Quality Systems

3. May 2027

Process Validation

10. May 2027

ISO 13485 and Quality Management for Medical Devices / Internal Auditing

13. May 2027

Generating Clinical Evidence for Medical Devices using 14155 and ISO 18969

20. May 2027

Medical Device Usability

24. May 2027

Design Control

9. June 2027

Medicovirksomheders behandling af personoplysninger – juridiske og praktiske udfordringer

10. June 2027