Medical Device EU MDR Seminar
Sep 30, 2025
By Dana Tirosh B.A.
Cycle 14.0
Regulation
Starts at: 09:30
Duration: 1 Meetings
Language: Hebrew
This one-day seminar offers a comprehensive, practical overview of the MDR framework, covering regulatory obligations, conformity assessment, documentation, and post-market surveillance. Participants will gain clarity on the transition from MDD to MDR and learn how to navigate the updated requirements efficiently.
Through real-world examples and lessons learned, the seminar equips attendees with applicable tools to improve compliance and avoid common pitfalls.
Whether you're planning for certification, in the middle of the transition, or supporting MDR implementation, this course offers essential insights and actionable knowledge.
About Dana Tirosh B.A.
Regulatory and Quality expert and a certified lead auditor (BSI Certified Lead Auditor - ISO 13485:2016 IRCA Certified) Experienced in establishing, implementing and maintaining a QMS, well familiar with international standards and regulations, audit management, project oversight and Global Regulatory Submissions. Successfully participated in many ISO 13485, EU and MDSAP Audits as the lead point of contact. Dana is...
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This seminar focuses on the practical application of regulatory tools and pathways available through the EU market, using real-world examples and exercises to help you understand the regulations and how to comply with them effectively.