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