Free webinar — How to conduct usability engineering under the EU MDR

Presenter (in English): Kristina Zvonar Brkic

Kristina Zvonar Brkic
Webinar designed for companies and managers who need to conduct usability engineering for medical devices under the European Union Medical Device Regulation. It shows the basics, key factors, and documents needed to become compliant.

Upcoming Dates/Times:

Thursday – June 6, 2024

11:00 AM New York time

4:00 PM (16:00) London time

5:00 PM (17:00) Brussels time

11:00 PM (23:00) Perth time

Duration: 1 hour / Convert to your time zone

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Register for this webinar to learn:

  • What is usability, and what are the keywords?
  • Why is it necessary to conduct usability engineering?
  • What regulations are applicable?
  • What kind of errors are there while using a medical device?
  • What is formative evaluation?
  • What is summative evaluation?
  • Which documents are necessary?

What you will receive:

  • Training delivered by Kristina Zvonar Brkic, one of the leading experts for EU MDR & ISO 13485
  • Access to webinar recording

Target audience:

This training is designed for team members responsible for medical device technical documentation, including:

  • Quality managers
  • Production managers
  • Sales managers
  • Persons responsible for regulatory requirements
  • CEOs
  • Owners
  • Complaint managers

About the training:

10 steps to achieve MDR compliance [free webinar]

This live, interactive online training (via webinar) is designed to enable you to walk away with knowledge and understanding of key factors for usability engineering under the EU MDR. This course offers compelling content, a downloadable presentation deck, and live engagement with an expert consultant with whom you can discuss how to resolve your specific implementation issues. You will experience the training right from your desk, eliminating travel costs and minimizing lost time away from your office.

Presented by: Kristina Zvonar Brkic

Kristina Zvonar BrkicKristina Zvonar Brkic is an experienced consultant, auditor, assessor, and trainer for ISO 13485 and the EU MDR. She runs a thriving ISO 13485 consulting practice and helps companies and consultants to build their businesses. In her career, she also worked as an ISO 9001 and ISO 22716 consultant and lead auditor, and an auditor and assessor for MDD.

The portfolio of medical devices for which she has approval includes plastic products with measuring function, various creams and gels, different systems for wound care, disinfectants, dental materials, different catheters, panels for operating rooms and clean rooms, accessories, kits for performing surgical procedures of non-woven materials, and medical gases.

Related Frequently Asked Questions

In which language are the webinars delivered?

Live online trainings via webinars are currently delivered in English only. However, we plan to deliver some of the trainings in other languages, too.

Are these trainings held in person, at a specific venue?

No, all our live online trainings are delivered through Internet only, via webinars. Webinars enable you to experience both audio and video presentation from our presenter/trainer.

What do I need to watch the webinars on Demand (recording of live online streaming)?

You just need your computer with a browser - webinar recordings can be watched as any other video on the internet, e.g. on YouTube.

How many times can I watch the webinar recordings?

The number of views is not limited - you can watch the recordings as many times you wish.

About 13485Academy

 

13485Academy is one of the Academies of Advisera.com. Advisera specializes in helping organizations implement top international standards and frameworks such as EU GDPR, ISO 27001, ISO 9001, ISO 13485, ISO 14001, ISO 45001, IATF 16949, ISO/IEC 17025, AS9100 and ISO 20000. Over the years, Advisera has become a global leader in the provision of web-based training and documentation developed by the leading experts.

Our products are of best-in-class quality. With a proven performance record of successful implementations in more than 100 countries, our world-class customer support ensures success. Read more about the 13485Academy here.

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