Effective Internal Auditing-Making Quality Systems More Efficient for the Medical Products Industry - Webinar By GlobalCompliancePanel 2011

  • 11 Oct 2011
  • Webinar

Description

Topics
  • Defining Internal Auditing
  • Quality 101
  • Auditor Qualifications
  • Objectives of Internal Auditing
  • The Audit Lifecycle
  • Auditing Responsibilities
  • The Internal Audit Report
  • Value Added Auditing
  • Confidentiality of Audit Reports
Who should Attend
  • Interdepartmental functions associated with scaling up and commercializing a new medical product
  • Quality control, Quality, engineering, regulatory, IT and manufacturing staff working in the FDA regulated industry in the development and manufacture of medical products
  • Suppliers and software vendors, servicing the FDA regulated industries, who want to better understand the customer’s needs and requirements
  • Regulatory Affairs working on approval of combination products

Past Events

Important

Please, check "Effective Internal Auditing-Making Quality Systems More Efficient for the Medical Products Industry - Webinar By GlobalCompliancePanel" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations
Health & Medicine: Medical device, Pharma

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