Frequently asked questions for the Medical Device Single Audit Program (MDSAP)

Name: Frequently asked questions for the Medical Device Single Audit Program (MDSAP)
Creator: Therapeutic Goods Administration
Keywords: audits,faq,frequently-asked-questions,manufacturers,mdsap,medical-device-single-audit-program,medical-devices,q-a,questions-and-answers,sponsors

Information

Original link

Type

Page

Regulated products

Medical Devices

Published

October 26, 2023

Last updated

December 1, 2023

Description

Read our questions and answers for sponsors and manufacturers about the Medical Device Single Audit Program (MDSAP).

Organization

Therapeutic Goods Administration (TGA) 🇦🇺

Country / Region

Australia

License

Other (Non-Commercial)

Feedback

Suggest an improvement to this page

1 Main file

Frequently asked questions for the Medical Device Single Audit Program (MDSAP)

Updated on December 1, 2023

html

URL: https://www.tga.gov.au/how-we-regulate/manufacturing/manufacture-medical-device/medical-device-single-audit-program-mdsap/frequently-asked-questions-medical-device-single-audit-program-mdsap
Permalink: https://data.openrid.co/en/datasets/r/a0e13bab-7b06-4507-add7-276f8dcaad16
MIME Type: text/html

Created on: October 26, 2023
Modified on: December 1, 2023

Frequently asked questions for the Medical Device Single Audit Program (MDSAP)

Information

Type

Regulated products

Published

Last updated

Description

Tags

Organization

Country / Region

License

Feedback

Actions

Social networks

Embed