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  1. Design History File (DHF), the Device Master Record (DMR) and the Device History Record (DHR) ? Principles on Lean Documents and Lean Configuration By Jose Mora
  2. CAPA Training and Causes of Warning Letters due to Lack of Comprehension By Jerry Dalfors
  3. 6-hr Virtual Seminar: Latin America ? Understanding Regulatory Compliance Requirements Across the Life Science Industry By Robert J. Russell
  4. Conducting an Effective Quality System Management Review By Michael Brodsky