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Event Serial: WCA405814
Contact Person – Yuliia Terletska
Event inquiry /Organizer email address – yuliia.terletska@uventia.com
Organized by: Uventia Global
Topic Covered: Medicine and Medical Science, Management, Business, Marketing, Distance Education, Higher Education, Bioinformatics, Biotechnology, Engineering, Manufacturing, Networking
Event Start Date – 23rd May 2022
Deadline For Abstracts/Proposals: 20th May 2022
Event End Date -24th May 2022
Venue: Prague , Czech Republic
About Event:
Our virtual meeting proposes the actions medical device manufacturers could take to strengthen the implementation strategy for EU MDR and IVDR. The expert speakers will share all the different ways to prepare your company and team for a smooth transition; your QMS for EU MDR; meet Notified Body expectations during the audit; comply with requirements for vigilance reporting and post-market surveillance; review labeling and packaging challenges under d UDI; evaluate strategies to remediate gaps in clinical data and more.
Website: https://www.uventia.com/event/medical-device-regulations-summit-2022/
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