If you would like to join our Qualtech Webinar on the topic of the “EU MDR”, please access the webinar by using the following link and passcode:

Zoom Webinar Link: https://us02web.zoom.us/j/86359838298?pwd=aXZkMjY0Zmk1eEFwU1dDcHgzSFB4dz09
Passcode: 567106

Webinar ID: 863 5983 8298

Please be aware that the online event will take place on Tuesday, February 7th at:
- 5:30pm to 6.30pm local Japan Time (GMT+9)
- 4:30pm to 5.30pm local Taiwan Time (GMT+8)
- 9:30am to 10.30am Central European Time (CET/GMT+1)


Enter EU market with confidence: Keep updated on MDR Regulation changes! Join Qualtech MDR webinar on 07 Feb 2023 (Tue) at 16:30 – 17:30 p.m. (GMT+8).

A perfect opportunity to prepare for the changes and minimize the impact on you.


Webinar Agenda:

EU MDR 2017/745 update

System readiness and latest developments

•MDR implementation state of play

•Insights from MDR reviews

•Annex XVI common specifications for non-medical purpose devices

•What is next - Q&A


Speaker Arkan Zewick’s Background:

Mr. Arkan Zwick is Corporate Regulatory Affairs Director of Croma. Arkan has a graduate master degree in Law from the University of Vienna and a PhD in European Law. Arkan´s role in Croma includes regulatory advocacy for drug, medical device and cosmetic compliance projects as well as in house legal advice for contract management, merger and acquisition and intellectual property projects.

He is responsible for the company’s regulatory compliance in the EU working with several notified bodies and for global market authorizations in the United States and Asia-Pacific. Arkan has more than 10 years of experience in medical device regulation, it will be precious opportunity for him to share with all of you on MDR regulation updates.


Register Today!

To register the webinar, please click here and complete the form before the space runs out.

A confirmation email will be sent to you after filling in the form. Please contact us, if do not receive any email after the first week of February.

Do not hesitate to reach out if you have questions, comments, or concerns regarding this webinar.


We look forward to seeing you online