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Free webinar - Post-Market Surveillance System According to the EU MDR Requirements

Overview

The purpose of this webinar is to help you meet the key requirements of your company’s post-market surveillance (PMS) under the EU MDR 2017/745 and explain how to integrate them with the QMS.

Presenter (in English):
Kristina Zvonar Brkic

Lead Expert for ISO 13485
& EU MDR

Kristina Zvonar Brkic

Upcoming Dates/Times:

Tuesday – November 11, 2025

11:00 AM New York time

4:00 PM (16:00) London time

5:00 PM (17:00) Brussels time

Duration: 1 hour / Convert to your time zone

Can’t make the date? Watch the recording here.

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Register for this webinar to learn:

  • How the PMS system works
  • What regulating requirements are
  • Which documentation you need for integrating PMS requirements with the QMS
  • How PMS, risk management, and clinical evaluation are related

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 people at medical device manufacturers who are involved in post-market surveillance, including:

  • quality managers
  • production managers
  • sales managers
  • person responsible for regulatory requirements
  • CEOs
  • owners
  • complaint managers

About the training:

What is EU MDR and how can ISO 13485 help with compliance?This live, interactive online training (via webinar) is designed to enable you to walk away with knowledge and understanding of what the post-market surveillance process is expected to be, which regulation must be followed, and how to implement it with documentation within your QMS. 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 Brkic

Kristina 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 staging.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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