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 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.
09.12.2024
Seminar hours - 09:30-15:30
Location; Tel Aviv
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.