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.




Status Confirmed
Edition 2016 (2021)
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
Adoption -