Medical Devices Regulations: Europe Seminar
Gstudy > Courses and seminars > Medical Devices Regulations: Europe Seminar
Regulatory
Location: Frontal
Starts at: 09:30
Duration: 1 Meetings
Language: Hebrew
This seminar emphasizes the practical implementation of regulatory tools and pathways within the EU market. Through real-world examples and hands-on exercises, participants will gain a clear understanding of the regulations and learn how to achieve compliance efficiently and confidently.
All the Essentials You Must Know About the MDR!!
26.02.2025
Seminar hours - 09:30-15:30
Location; Matan Haifa
Price - 1,500 NIS + VAT
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.