Medical Device Single Audit Program (MDSAP)
Information
Type
Page
Regulated products
Medical Devices
Topics
In Vitro Diagnostic Medical Devices (IVDs)
Published
December 1, 2023
Last updated
December 1, 2023
Description
The MDSAP allows recognised organisations to audit device manufacturers in a single program that satisfies the requirements of the participating regulatory authorities.
Tags
Organization
Country / Region
Australia
License
Other (Non-Commercial)