Events

Seminar: Person responsible for compliance with the regulatory provisions according to MDR / IVDR

Wednesday December 14th
09: 00 - 16: 30
Online meeting

In this seminar, in addition to the regulatory framework, you will receive many practice-oriented tips and learn how the requirements can best be implemented.

Every manufacturer of medical devices must appoint at least one responsible person who knows the provisions of the new EU regulation and monitors compliance. Get the necessary knowledge about the areas of responsibility with this seminar!

What tasks do I have as the responsible person? How do I plan for long-term compliance with these requirements?

your coach
Daniel Rubisoier, BSc, MSc, Conformity Assessment Procedure Specialist MDR, TÜV SÜD Product Service GmbH

Registration is via en.co.tec. Please follow the registration button. 

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Seminar: Person responsible for compliance with the regulatory provisions according to MDR / IVDR
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costs and registration

This seminar takes place in cooperation with Human.technology Styria. Registration is via en.co.tec. Participation fee for HTS members: EUR 440 (excl. VAT)

didactics and methods

The didactic concept follows the principles of adult education. Learning takes place using application-oriented case studies. It is supported by keynote speeches, practical exercises, group work and discussions. Common methods are used by working with Power Point presentations, flip charts, pin boards, etc. Methods and tools for practical implementation are taught.

Certificate of Participation

Before the start of the course, the participants will be informed about what must be achieved in order to obtain a confirmation and in what form the learning outcomes will be checked (active participation, practical exercises, group work, discussion groups, test). The participants have to fill out a feedback form with questions about the workshop.

What else should you know?

All you need for our ONLINE seminars is a laptop with a camera and microphone. Our eLearning platform works on all operating systems in the web browser (e.g. Firefox, Safari or Chrome). You will receive the seminar documents and the link to the virtual seminar room in good time by email.

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The seminar will be designed interactively - similar to a face-to-face seminar: ie you can ask your questions to the lecturer, there will be practice examples and also the opportunity to exchange ideas with the other participants.

Contact HTS

Michael Pichler
+43 699 18899 707
michael.pichler@human.technology.at

Seminar content

Preface
– General, purpose, regulation, definitions
– Legacy device, transitional provisions

Person responsible for regulatory compliance
– Qualifications, responsibilities, availability
- Liability

Technical Documentation
Annex II: structure including content
– Annex III: Post-Market Surveillance System, Vigilance, Market Surveillance

Conformity assessment
– Annexes IX, X, XI

EU declaration of conformity
Appendix IV