Transform critical requirements for your medical device into a relevant product

Become an expert in medical product development using the unique combination of regulatory, reliability, design for six sigma, data analytics and project management.

View course calendar
Talk to our academy advisor
TechMed-Event-600x401

Develop your medtech competences.

CE certification of medical device - opening image

Quality management systems

Learn how to set up a complete ISO13485 compatible quality management system from scratch, extend an ISO9001 system or complete gap analyses.
HI way of working

Regulatory requirements

Easily create the technical documentation for your medical device, from drafting requirements to clinical evaluation.
057

Medical design for six sigma and data analytics

By applying proper statistical analysis, ensure that your verification and validation results are reliable and useful.
https://www.holland-innovative.nl/hubfs/lisette-1-1.jpg
The MedTech courses offered by Holland Innovative are a good representation of our belief that a pragmatic and comprehensive approach in this sector yields the best results.

Lisette van Steinvoren - Stamsnijder

Competence Lead MedTech - Holland Innovative

MedTech Courses

HI-MT3 In Vitro Diagnostic Medical Devices - Getting started with CE Certification

Courses for MedTech professionals MedTech

Get an overview of the regulatory requirements and learn how to implement these in your development process.

Lisanne Karbaat
Lisanne Karbaat
Regulatory Affairs Expert IVDR
  • 1 day

HI-MT2 Medical Devices - Getting started with CE Certification

Courses for MedTech professionals MedTech

Get an overview of the regulatory requirements and learn how to implement these in your development process.

Lisette van Steinvoren - Stamsnijder
Lisette van Steinvoren - Stamsnijder
Competence Lead MedTech & Sr. Project Manager Medical
  • 1 day

HI-MT8 Clinical Evaluation and Data analysis – for Medical Devices

Courses for MedTech professionals MedTech

Designed for medical device professionals, this training increases knowledge and understanding of clinical evaluation and post-market surveillance (PMS), and enables you to integrate clinical evaluation into your product development processes.

Monique van Lier
Monique van Lier
Medical Device Development Expert
  • 1 day

What we believe works.

In 15+ years of practice, we have generated a clear vision of what competences are needed in different business environments and job roles.

Get started

Get started and save your seat.

Take the next step in your personal development.

Talk to our academy advisor
View academy calendar