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

Description

Compliance Risk Management in Medical Devices, Pharmaceuticals, and Combination Products is a conference that covers topics such as:

  • 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

Compliance Risk Management in Medical Devices, Pharmaceuticals, and Combination Products brings together:

  • 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

Future Events

Compliance Risk Management in Medical Devices, Pharmaceuticals, and Combination Products 2020

Important

Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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