Convention · Irvine, California
Integrating a Quality Management System and Risk Management for Medical Devices
Education, Training · Medicine · Life Sciences
Key numbers
- Editions on record
- 1first in 2011
About Integrating a Quality Management System and Risk Management for Medical Devices
This 2 days ComplianceOnline seminar covers the essential elements of a medical device quality management system involved in creating an effective Risk Management system. Using ISO 13485 as a model, the seminar covers the QMS essentials that have the most direct impact on Risk Management. These QMS activities include product planning, design and development, supplier management, process validation, customer complaints, internal quality audits, corrective action, preventive action, and post-market surveillance. In addition, the seminar clarifies the requirements for verification and validation. The material compares and contrasts ISO 13485 and FDA QSR requirements.
From our listing of this edition. Details may have changed since.
Editions
| Year | Dates | Where | Exhibitors | Visitors |
|---|---|---|---|---|
| 2011 | 24–25 Feb 2011 | Hilton Irvine/Orange County Airport Irvine, California | — | — |
Past editions from the bvents archive (2008–2019) and organiser figures where they were published.
Questions
When is Integrating a Quality Management System and Risk Management for Medical Devices?
The next dates haven't been confirmed. The last edition we have on record was 24–25 Feb 2011.
Where is it held?
The last edition we have was at Hilton Irvine/Orange County Airport, Irvine, California.