Risk-based Supplier Management System: ImpactImpact on Regulatory and Operational Goals for Medical Device Manufacturers 2015

  • 30 Sep 2015
  • Online Event

Description

Risk-based Supplier Management System: ImpactImpact on Regulatory and Operational Goals for Medical Device Manufacturers 2015 covers topics such as:

  • Learn about the two guidelines that cover current FDA and ISO 13485 expectations for supplier control
  • Understand the types of suppliers that must be qualified according to the FDA and ISO 13485
  • Understand how to create or bring your supplier program into compliance with the these guidance documents while optimizing the resources needed to comply
  • Understand how to use the Global harmonization Task Forces (GHTF) and NBOC supplier guidance documents that you could be audited to
  • Understand how to define and control supplier risk and why this benefits your company
  • Understand requirements for Critical suppliers
  • Learn about best practices for supplier qualification and control

Risk-based Supplier Management System: ImpactImpact on Regulatory and Operational Goals for Medical Device Manufacturers 2015 brings together attendees from:

  • Regulatory Affairs
  • Quality Management
  • Supplier Engineering
  • Supply-Chain Management
  • Supplier Auditing
  • Purchasing Management
  • Quality Engineering
  • Internal Auditing

Past Events

Important

Please, check "Risk-based Supplier Management System: ImpactImpact on Regulatory and Operational Goals for Medical Device Manufacturers" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Human Resources (HR), Risk Management
Health & Medicine: Medical device, Medical technology

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