for medical devices & in vitro diagnostics according to MDR / IVDR
The technical documentation is the fundamental prerequisite for product approval as a medical device or in vitro diagnostic. This seminar explains step by step how the technical documentation should be structured in order to meet all the requirements of the new EU regulations (MDR / IVDR).
The seminar contents
- Overview of the requirements of the EU regulations (IVDR / MDR)
- Structure and content of the technical documentation
- Essential requirements
- Cross-section of the most important harmonized standards
- Practice Examples and Practical Tips
Costs
1 day in-house training: € 3,890 (excl. VAT) for max. 10 participants
incl. seminar documents and certificate of attendance, plus travel expenses
your trainer
DI Martin Schmid, Managing Director & Senior Consultant en.co.tec
Information about our trainers
Book now:
Please send your request to seminare@encotec.at or call us: +43 1 8863491 +43 1 8863491
