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Quality Audits for the Medical Device Industry 2017
02-03 Mar 2017
San Diego, CA, United States
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Quality Audits for the Medical Device Industry 2017
Key Topics
The difference among audit methods (system, product, process, etc.)
Learn the difference among the audit types
The role of auditor competency and how to determine it
Audit scheduling and methods to establish and update the schedule
The role of correction and corrective action related to an audit nonconformance
Which audits an auditor could conduct and which ones to avoid
Develop an effective approach for reporting at management review
Who should Attend
Attendees from:
Lead Auditors
Audit Managers
Management Representative
Audit Team Members
Quality Engineers
Quality Assurance Managers
Supplier Management and Purchasing
Regulatory Affairs Managers
Supplier Quality Engineers
Read more
Past Events
Quality Audits for the Medical Device Industry 2017 - 02-03 Mar 2017, San Diego, California, United States
(65551)
Quality Audits for the Medical Device Industry 2016 - 01-02 Dec 2016, The Westin San Jose, California, United States
(63656)
Quality Audits for the Medical Device Industry 2026
Important
Please, check "Quality Audits for the Medical Device Industry" official website for possible changes, before making any traveling arrangements
Event Categories
Business:
Facility planning & Management, Finance, Internal Audit & Compliance, Management, Quality assurance
Health & Medicine:
Hospitals & Clinics, Medical device, Medical laboratories, Medical technology
Technology:
Information Technology (IT)
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