2021 - Lead Auditor EN ISO 13485:2016 and EU MDR 2017/745 - Regulation
Date2021-07-12 - 2021-07-13
Deadline2021-07-02
VenueVirtual Seminar, USA - United States
KeywordsEU MDR 745/2017; EN ISO 13485:2016; Iso 13485 2016 standard
Topics/Call fo Papers
The new scope of the EU MDR 2017/745
The obligations and roles of the EU MDR 2017/745
How work the regulation and the EN ISO 13485:2016 together?
New and updated processes required by the EU MDR 2017/745
How to implement the required changes until May 2021?
The obligations and roles of the EU MDR 2017/745
How work the regulation and the EN ISO 13485:2016 together?
New and updated processes required by the EU MDR 2017/745
How to implement the required changes until May 2021?
Other CFPs
- Biostatistics for the Non-Statistician
- I International Scientific and Theoretical Conference «The current state of development of world science: characteristics and features»
- Writing and Revising SOPs for Increased Operational Efficiency
- Human Error Reduction in GMP Manufacturing
- Complaint Management: Best Practices to Assure Regulatory Compliance and Customer Retention
Last modified: 2021-05-18 11:29:16