Healthcare Medical Software/Applications - Risks, Validation & Interoperability 2017

  • 06 Jun 2017
  • Webinar

Description

The Healthcare Medical Software/Applications - Risks, Validation & Interoperability 2017 is a webinar that covers topics such as:

  • Risk based classification
  • Current regulatory approaches
  • Future regulatory strategy
  • Proposed regulation and guidance
  • Premarket requirements
  • Impact of regulation
  • Marketing boundaries
  • Post market requirements
  • Enforcement action
  • Regulatory action
  • Design and validation
  • Quality Systems regulation
  • Required regulatory reporting
  • Corrective and preventive actions
  • Regulatory scope
  • Medical Device Data Systems (MDDS)
  • Implementation issues
  • Device classification criteria
  • Interoperability issues
  • Industry issues
  • Servicing
  • Device interface
  • Mobile Applications
  • Professional and consumer use

The Healthcare Medical Software/Applications - Risks, Validation & Interoperability 2017 is intended for:

  • Senior Managers of Manufacturing Operations
  • Medical Device Software Design Engineers
  • Managers for software based medical devices
  • Regulatory Affairs Auditors
  • Sales and Marketing
  • Risk Managers
  • Institutional and Clinical Software Users
  • Software Vendors
  • Cyber Security Manager

Past Events

Important

Please, check "Healthcare Medical Software/Applications - Risks, Validation & Interoperability" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Risk Management
Health & Medicine: Healthcare, Medical device, Medical technology

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