5.3.17 Screening administrative data Global Trigger Tool

Purpose and goal

Patients have the unrestricted right to be informed about adverse events and the circumstances that may have led to them. At the very least, there is an obligation to provide information upon the patient's request or if the information is necessary to avert health risks)

BGB §630c para. 2 sentence 2; QM-RL §4 (1) Patient information and education sentence 1; DIN EN ISO 9001:2015 and DIN EN 15224:2017 8.2.1 i)

Area of application

In the event of adverse events (AEs) during or after treatment, in particular if a treatment error is suspected as the cause of the AE.

Description of the

Attachments