Free webinar – Overview of the Steps Needed to Comply With EU MDR

Presenter (in English): Kristina Zvonar Brkic

Kristina Zvonar Brkic
Webinar designed for organizations that have medical devices that need to be certified according to the EU MDR. This webinar will help you understand the necessary steps that need to be taken, and requirements to be fulfilled, to be fully prepared for and in compliance with the EU MDR.

Upcoming Dates/Times:

Thursday – May 9, 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

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 MDR is and why it is needed
  • Steps for successful MDR compliance for certified medical devices
  • Deadlines for compliance
  • Exceptions for Class I medical devices (self-declaration)
  • List of documentation to be focused on

What you will receive:

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

Target audience:

This training is designed both for those who already have certified medical devices according to MDD and those who are planning for the first certification according to the MDR, including:

  • CEOs
  • Quality Managers
  • Persons responsible for technical documentation
  • Persons responsible for design and development of medical devices

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 on what needs to be prepared and done for on-time compliance with 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 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 for 7 years, and currently MDR.

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).

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.

100% Secure Online Billing

 

We use Secure Socket Layer (SSL) technology, the industry standard and among the best available today for secure online commerce transactions. All of your personal information, including credit card number, name, and address is encrypted so it cannot be read during transmission. You are protected by your credit card company in the case of a fraudulent transaction with any purchase.

cards

AES-256bit SSL safe Privacy Policy

Online payment services are provided by BlueSnap and 2Checkout.