The new EU regulations replace the EU directives for medical devices that have been in effect for more than 20 years.
With this practice-oriented in-house workshop, we aim to support you in identifying the topics of the new EU regulations for medical devices and IVDs that are relevant to you, and in jointly discussing and planning the specific impacts and necessary actions.
Take advantage of this offer to manage the transition systematically and in a timely manner!
program
- 1-day gap analysis of the relevant changes, new requirements, and specific impacts for your company → joint development of a transition strategy
- ½-day follow-up: Review and evaluation of the action plan you developed based on the jointly created transition strategy.
- Optional: ½-day training on MDR / IVDR (on selected topics / for participants with prior knowledge)
We are also happy to support you in implementing the action plan.
Costs
- 1.5 days on-site at your location with one of our experts: Euro 3,890 (excluding VAT).
- 2 days on-site at your location with one of our experts: Euro 4,490 (including ½-day training)
Book now:
Please send your request to seminare@encotec.at or call us: +43 1 8863491 +43 1 8863491
