Compliance Risk Management in Medical Devices, Pharmaceuticals, and Combination Products 2019

  • 07-08 Feb 2019
  • Tampa, FL, United States

Description

Topics
  • What Is Compliance Risk Management? Where is this occurring today? What are we going to have to do differently?
  • Introduction to Risk Management since the 1980’s
  • Acceptability Criteria – Do’s and Don’ts
  • Various Solutions for Implementing Compliance Risk Management
  • The Trace Matrix for Product and Compliance - Documenting Risk the Right Way, Improving EU Compliance Posture with Trace Matrix
  • Leveraging Risk Management to Potentiate Operational Excellence - The Concept of Positive Risk as Opportunity, Cost Reductions, How to Justify Decisions
  • Benchmarking for the Future - Benchmarking for Objective Evidence to Management, How to Benchmark Effectively with Risk Management
Who should Attend
  • Quality professionals
  • Senior quality managers
  • Compliance professionals
  • Regulatory professionals
  • Manufacturing engineers
  • Production managers
  • Design engineers and managers
  • Production engineers
  • Quality engineers
  • Process owners
  • Document control specialists
  • Quality auditors

Past Events

Important

Please, check "Compliance Risk Management in Medical Devices, Pharmaceuticals, and Combination Products" official website for possible changes, before making any traveling arrangements

Event Categories

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

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