FDA Concepts for Medical Device Companies - Regulations, Myths, Challenges, and Best Practices – GlobalCompliancePanel 2016

  • 01-02 Dec 2016
  • DoubleTree by Hilton Baltimore - BWI Airport, Linthicum, MD, United States

Description

FDA Concepts for Medical Device Companies - Regulations, Myths, Challenges, and Best Practices GlobalCompliancePanel 2016 is a seminar that covers topics such as:

  • Regulations
  • Expectations for Medical Device Quality Management Systems
  • Lessons Learned
  • Quality Management System Structure and Processes
  • Challenges
  • Myths
  • Inspection Readiness
  • Best Practices

FDA Concepts for Medical Device Companies - Regulations, Myths, Challenges, and Best Practices GlobalCompliancePanel 2016 brings together:

  • Process Engineers
  • Quality Engineers
  • Compliance Specialists
  • Design Engineers
  • CAPA Specialists
  • Quality and Compliance Managers
  • Senior Management wanting an overview of Quality Systems and Management Responsibility
  • Auditors
  • Anyone wanting an introduction to Quality Management Systems

Past Events

Important

Please, check "FDA Concepts for Medical Device Companies - Regulations, Myths, Challenges, and Best Practices – GlobalCompliancePanel" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Quality assurance
Government & Global Issues: Law & Regulations
Health & Medicine: Healthcare, Medical technology

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