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ComplianceOnline Home > ComplianceOnline Standards > FDA Audit, Validation & Documentation – Checklist, Templates& master plans
 
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The purpose of this procedure is to establish a system of controlling Design and Development changes after a product has been released for production.
Provider: Quality Rite
Shipping: Available for download - Link will be provided in My ComplianceOnline section
Price: $25.00

Product Detail:

The purpose of this procedure is to establish a system of controlling Design and Development changes after a product has been released for production.

It Provides information on:

  • Responsibility.
  • Requirements.
  • Records.
  • Method.

Who will benefit:

  • Engineer Manager.
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