Groots In Vitro Diagnostic Expert can offer you various medical device trainings:

- Introduction to EN-ISO 13485
- Practical implementation of EN-ISO 13485
- EN-ISO 13485 Internal auditor
- Introduction to MDR
- Introduction to IVDR
- Practical implementation of MDR
- Practical implementation of IVDR
- Person Responsible for Regulatory Compliance
- Risk Management conform EN-ISO 14971
- Usability conform IEC 62366
- Biocompatibility conform ISO 10993
- Successful in 510(k) submissions
We can recommend you the excellence package as it will serve as an extra service to your organisation. During this extra day, we are able help you with e.g. an effectiveness check, gap-assessment, risk management activities for your new device or a practical implementation of the learned theory.
Do you want to have information about the available training dates or if you would like to have more in-depth information about the training itself or about the optional excellence package.
Contact our senior consultant Lizette