EU-IVDR Implementation 2020 - What You Need to Know: Auditing EU-MDR and EU-IVDR Implementation
Topics/Call fo Papers
With one extension already granted, any organization selling devices in the region now need to be ready for the shift by May 2021. There’s little time to spare to get your processes up to par — but WCS
Join us for the Live Webinar on Tuesday, October 27, and learn about Auditing EU-MDR and EU-IVDR Implementation.
The Internal Audit Program
ISO 19011:2018
ISO 13485:2016
Speaker:
David R. Dills, is an independent Global Regulatory Affairs & Compliance Consultant and has an accomplished record with more than 26 years of experience in regulatory affairs
Join us for the Live Webinar on Tuesday, October 27, and learn about Auditing EU-MDR and EU-IVDR Implementation.
The Internal Audit Program
ISO 19011:2018
ISO 13485:2016
Speaker:
David R. Dills, is an independent Global Regulatory Affairs & Compliance Consultant and has an accomplished record with more than 26 years of experience in regulatory affairs
Other CFPs
- Knock, knock, who’s there? Are you ready for an FDA inspection in the COVID-19 Era and Beyond?
- A Critical Step in Risk-Based Approach to CSV, 21 CFR Part 11 and FDA Compliance
- Sterilization of Pharmaceutical Products and Medical Devices During COVID19 New Course
- International Conference on Civil Engineering (CiViE 2021)
- 8th International Conference on Mechanical Engineering(Meche 2021)
Last modified: 2020-10-23 23:14:50