ISO 13485 and the Paperwork Behind a Qualified Marking Process

Pharma Manufacturing - The Sabreen Group, Inc

A marking process in a device quality system needs design controls, validation, traceability and change control. What each one asks for in practical terms.

Scott Sabreen
President & Chief Engineer
30+ Years of Expertise

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Medical & Pharmaceutical

ISO 13485 and the Paperwork Behind a Qualified Marking Process

Scott Sabreen President & Chief Engineer 30+ Years of Expertise

Scott Sabreen
President & Chief Engineer
30+ Years of Expertise