SS 620:2016 (2021)
Good distribution practice for medical devices - Requirements
This standard serves as a guide on the quality management system for the handling, storage, delivery, installation, servicing, secondary assembly and other related activities (e.g. warehousing, logistics and freight forwarding services) of medical devices including in-vitro diagnostic devices. It establishes the fundamental requirements that are to be met in order to ensure the quality and integrity of medical devices that are being imported and distributed in Singapore.
|No. of Pages||19|
|ICS Classification||03.100.70 Management systems
11.040.01 Medical equipment in general
|Committee||Biomedical and Health Standards Committee
|Available for Purchase||Global|