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.
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.
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
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- Sterilization of Pharmaceutical Products and Medical Devices During COVID19 New Course
- New FDA Proposed FSMA Rule on Food Traceability
Last modified: 2020-10-19 23:04:27