How to Implement MDSAP-Requirements into your ISO 13485
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Website https://www.compliance4all.com/control/w_product/~product_id=502397LIVE?channel=ourglocal_Apr_2019_S |
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Category Quality Management System, MDSAP-Requirements, ISO 13485, compliance trainings, Single Audit Program, quality management system guidelines, ich quality management system, fda quality management system
Deadline: April 13, 2019 | Date: April 15, 2019
Venue/Country: Online, U.S.A
Updated: 2019-02-18 15:33:10 (GMT+9)
Call For Papers - CFP
Overview:How a smart implementation of these requirements in the quality management system is possible and finally how the audit for five countries (Australia, Brazil, Canada, Japan, US) is working.Why should you Attend:Your implementation time should be short and need smart ideas to reach the right level to pass the MDSAP - Audit by your audit organization. Areas Covered in the Session:Which Companies must have MDSAP?Which Companies should have MDSAP?Which Companies should postpone MDSAP?What are the requirements of MDSAP?Who Will Benefit:CEO's of companies, which sell to Australia, Brazil, Canada, Japan or USRegulatory Affairs Managers of Companies, which sell to Australia, Brazil, Canada, Japan or USQuality Managers of Companies, which sell to to Australia, Brazil, Canada, Japan or USSpeaker Profile:Prof. Dr. h.c. Frank Stein medical engineer, medical engineering experience since 25 years, clinical and research experience in cardiac surgery and cardiology, industrial experience in ophthalmology, neurology, traumatology and dental implants, active implants, active devices, international project and regulatory consulting experience in Europe, North-America, Asia, Australia, Arabic Countries, Latin-AmericaEvent Fee: One Dial-in One Attendee Price: US $150.00Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: compliance4all14gmail.com
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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