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TS16949 Certification Excludes 7.3 Product Design. Should Exclusion Be Stated?

Investigating the Cause of Corrective or Preventative Actions

Does this simple statement cover the needs of ISO 9001:2008 (8.5.3 Preventive Action)?

I am the “overseer” of the QMS, is this considered to be conflict of interest or the auditor auditing their own work?

Corrective and Preventive Action in ISO 9001:2008 and API Spec Q1

Finding the ISO 13485:2012 Standard

Format for Identifying Environmental Aspects

ISO – Certified vs. Registered?

Disposing of Solvent Waste

Quality Manual vs. Quality Plan?