This international standard addresses good clinical practices for the design, conduct, recording and reporting of clinical investigations carried out in human subjects to assess the safety and performance of medical devices for regulatory purposes. However, it does not apply to in vitro diagnostic medical devices.
Below you find the impact areas within the Responsibly Impact Parameter Framework which are covered by this data source.
Product safety
Social impact parameter
Quality assurance
Quality parameter
2
ESG TOPICS
Social
1
Quality
1