How to develop or update an internal auditing system that is compliant with FDA cGMP/ Quality System Regulation and ISO 13485, yet makes efficient use of company resources
The basic requirements of FDA cGMP/ Quality System Regulation and ISO 13485 which are the basis for what must be audited in your internal audit program
The difference between internal and external audits
How to manage an internal audit system
How using a risk -based process can make your audits more efficient and effective
How the internal auditing system can add value to your quality system and your company
What makes a good internal audit
How an effective audit system can be an integral part of continuously improving your quality system and your company
And have a chance to practice how to write effective audit non-conformances
And have a chance to practice the skills required for an internal or supplier auditor
What the FDA must see to verify that you are conducting your internal audits as required
Who should Attend
Attendees involved or interested in performing or managing audits of medical device quality management systems, including:
Quality professionals
Senior quality managers
Internal or supplier auditors
Regulatory professionals
Audit managers
New internal or supplier auditors
Past Events
Effective and Efficient Internal and Supplier Quality System Auditing for Medical Devices 2016 - 10-11 Nov 2016, Courtyard Jersey City Newport, New Jersey, United States (59647)
Important
Please, check "Effective and Efficient Internal and Supplier Quality System Auditing for Medical Devices" official website for possible changes, before making any traveling arrangements
