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Internal Auditing for the Medical Device Industry 2016
19-20 May 2016
San Francisco, CA, United States
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Internal Auditing for the Medical Device Industry 2016
Description
Topics
Types of audits, auditor qualifications, ethics, responsibilities, audit phases, audit planning, and scheduling
Overview of an auditing program, principles of quality management systems and how they related to auditing, benefits of auditing, and what is auditing
Auditing production, validation, and preservation. inspection and testing, control of test equipment, customer property, and sterilization
Auditing order handling, design control, purchasing, and supplier controls
Who should Attend
Attendees from:
Quality Manager
Who Will Benefit:
Quality Engineer
Quality Associate
Regulatory Associate
Quality Technician
Past Events
Internal Auditing for the Medical Device Industry 2016 - 19-20 May 2016, San Francisco, California, United States
(58526)
Important
Please, check "Internal Auditing for the Medical Device Industry" official website for possible changes, before making any traveling arrangements
Event Categories
Business:
Internal Audit & Compliance, Quality assurance, Risk Management
Health & Medicine:
Medical device, Medical laboratories, Medical technology, Pharma
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Event Reviews
"I was part of this seminar.The speaker was excellent stuff on this topic. It Very informative....!!!!!!!"
*****
Jason Warn, Researcher, Bybee Produce, United States (26-May-2016)
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