***Update***
Join us tomorrow, January 25, at 5 PM Taiwan Time or 10 AM CET for our FREE Webinar on MDR update 2024: System readiness, transition, next steps. Expand your knowledge with expert insights from Dr. Arkan Zwick, the Regulatory Affairs Corporate Director at Croma-Pharma GmbH.
Use this link and we will see you there!
Qualtech Consulting Corporation would like to invite you to join our upcoming webinar on MDR update 2024: System readiness, transition, next steps. This webinar will provide you with the latest information on EU Medical Devices Regulation 2017/745 and Regulation 2022/2346 on aesthetic purpose devices, and what manufacturers need to know to comply with them.
Date: January 25, 2024 (Thu)
Time: 5 PM Taipei Time or 10 AM CET
Speaker: Arkan Zwick, Regulatory Affairs Corporate Director at Croma-Pharma GmbH, Austria
Language: Conducted in English, with Chinese summary
Save your seat! https://forms.gle/BzWkUYZxskLyApKt7
- About the Speaker
- • Responsible for Croma-Pharma GmbH’s regulatory compliance in the EU
- • Obtained the MDR Annex XVI approval for CROMA dermal filler within 13 months.
- • More than 15 years of regulatory professional experience.
- • In-charge of the global market authorizations in the Americas and Asia-Pacific.
- • Has a graduate master’s degree in law from the University of Vienna and a PhD in European Law.
- • Has been assigned as lecturer at the University of Applied Sciences in Vienna, Austria.
About the Webinar
- • What manufacturers need to know on EU Medical Devices Regulation 2017/745
- • What’s next in 2024?
- • Regulation 2022/2346 on aesthetic purpose devices.
Don't miss this chance to get the MDR updates and successful experience in the registration of aesthetic purpose devices.
Register Now! And secure your spot for this informative and valuable webinar.
We look forward to seeing you online.
Please feel free to contact us for any question.