Free webinar – EU MDR Extra Requirements for Quality Management Systems not Covered in ISO 13485

Presenter (in English): Kristina Zvonar Brkic

Kristina Zvonar Brkic
The purpose of this webinar is to help you bring your company’s ISO 13485 Quality Management System into compliance with the MDR requirements for the QMS.

Upcoming Dates/Times:

Thursday – March 7, 2024

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.

REGISTER NOW
TO INTERACT DIRECTLY WITH AN EXPERT

You may unsubscribe at any time.

For more information on what personal data we collect, why we need it, what we do with it, how long we keep it, and what are your rights, see this Privacy Notice.

Register for this webinar to learn:

  • What the additional requirements are
  • How to implement them
  • What documents are needed

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 managers and personnel who need to align their organization’s ISO 13485 QMS with the EU MDR requirements, including:

  • Persons responsible for regulatory compliance (PRRC)
  • Quality managers
  • Personnel responsible for ISO 13485

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 of how to prepare your ISO 13485 Quality Management System to comply with MDR requirements for the 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 BrkicKristina Zvonar Brkic has worked as a consultant and lead auditor for ISO 9001, ISO 13485, and ISO 22716 for more than 10 years, and as an auditor and assessor for medical devices under MDD (now MDR) for seven years.

The portfolio of medical devices for which she has approval are as follows: plastic products with measuring function (spoons and syringes for giving antibiotics, cups and bags for urine), various creams and gels, different systems for wound care (vacuum-assisted therapy, different types of gauze, viscose and cellulose products, sponges and foams), disinfectants, dental materials, different catheters (infusion, transfusion, and urine), panels for operating rooms and clean rooms, accessories and kits for performing surgical procedures of non-woven materials, medical gases, and different dental materials (artificial teeth, filling components, and tips for aspirators).