Guideline

The following guideline can be ordered through the address listed in the "Source/Publisher"-category.
In cases in which you can order through the Internet we have established a hyperlink.

Medical Devices Post Market Surveillance: Global Guidance for Adverse Event Reporting for Medical Devices
Internet:	http://www.ghtf.org/documents/sg2/SG2-N54-R8-2006-Proposed.pdf
Origin/Publisher:	GHTF
Content:	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.