Effective and Efficient Internal and Supplier Quality System Auditing for Medical Devices: 2-day In-person Seminar

• Do you want to understand how to do efficient and effective internal and supplier audits that meet all the requirements of your external auditors, but also add value to your company?
• Are you confused by all the requirements and guidance documents for medical device quality management systems and are tired of wading through all the regulatory language they contain?
• Do you need to train new auditors for your medical device quality management systems or to audit your suppliers?
• Do you need to improve the training of your internal and supplier auditors so that they add value to these audits?

This course is designed for people who perform or manage audits of a medical device quality management system, including internal and/or supplier audits. Both 21 CFR 820 Quality Systems Regulation (cGMP), and ISO 13485 and Quality Management Systems auditing will be covered.

• Senior quality managers
• Quality professionals
• Regulatory professionals
• Internal or supplier auditors
• New internal or supplier auditors