Medical Device Registration and Approval IN KSA


The registration requirements carries elements from both Global Harmonization Task Force (GHTF). Devices shall comply with the relevant regulatory requirements applicable in one or more of the jurisdictions of Australia, Canada, Japan, the USA and the EU/EFTA, and additionally with provisions specific to the KSA to obtain registration approval.

Designed By Mohmmad Alahmad 2020. All rights reserved.