Risk Management in Medical Devices Industry (Jun 22 - 23, 2017)

Risk Management in Medical Devices Industry is organized by GlobalCompliancePanel and would be held during Jun 22 - 23, 2017 at Embassy Suites Boston Logan Airport, Boston, Massachusetts, United States of America.

The target audience for this medical event are Senior Quality Managers, Quality Professionals, Regulatory Professionals, Compliance Professionals, Project Managers, Design Engineers, Software Engineers, Process Owners, Quality Engineers, Quality Auditors, Medical Affairs, Legal Professionals.

Gaps, incorrect or incomplete implementation of software can delay or make the certification/approval of medical products impossible. Most activities cannot be retroactively performed since they are closely linked into the development lifecycle. Diligent, complete and correct implementation of risk management from the start of product development is therefore imperative. This course will introduce all necessary steps to design, implement and test critical medical device software in a regulatory compliant environment. Software risk management has to be embedded into the bigger scope of overall risk management. Therefore this course will additionally address the system level risk management and the resulting interfaces to software.

Additional Details will be posted as soon as they are available.