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 can help get you there.
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, compliance and quality consultative services
There’s little time to spare to get your processes up to par — but WCS can help get you there.
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, compliance and quality consultative services
Other CFPs
- Analytical Method Validation and Transfer According to the New FDA Guidance Training
- What You Need to Know IEC 62304 and Demystifying Software Validation using the Principles of LDLC
- Incorporating Coaching Methods Into Performance Management
- Aligning Corporate & Order to Cash Strategies
- 2nd International Conference on Machine Learning and Human-Computer Interaction (MLHMI 2021)
Last modified: 2020-11-05 18:49:26