Medical Devices Post Market Surveillance: Global Guidance for Adverse Event Reporting for Medical Devices

Titel:
Medical Devices Post Market Surveillance: Global Guidance for Adverse Event Reporting for Medical Devices
Herkunft/Verlag:

GHTF

Inhalt:
The objective of the adverse event reporting and subsequent evaluations is to improve protection of the health and safety of patients, users and others by disseminating information which may reduce the likelihood of, or prevent repetition of adverse events, or alleviate consequences of such repetition.

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