Requirements for Post-Market Surveillance of Medical Devices (MDS – REQ11)

Name: Requirements for Post-Market Surveillance of Medical Devices (MDS – REQ11)
Creator: Saudi Food and Drug Authority
Keywords: medical-devices,pms,post-market,post-market-surveillance,regulations,requirements,surveillance

Information

Type

Regulation

Regulated products

Medical Devices

Published

March 28, 2023

Last updated

March 28, 2023

Description

Regulation outlining requirements for post-market surveillance of medical devices.

Organization

Saudi Food and Drug Authority (SFDA) 🇸🇦

Country / Region

Saudi Arabia

License

Other (Public Domain)

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Requirements for Post-Market Surveillance of Medical Devices (MDS – REQ11)

Updated on March 28, 2023

pdf

URL: https://www.sfda.gov.sa/sites/default/files/2023-05/MDS_REQ%2011_V2_En.pdf
Permalink: https://data.openrid.co/en/datasets/r/bcea5153-dcb2-4830-9b64-db0e4774d4ad
MIME Type: application/pdf

Created on: March 28, 2023
Modified on: March 28, 2023

Requirements for Post-Market Surveillance of Medical Devices (MDS – REQ11)

Information

Type

Regulated products

Published

Last updated

Description

Tags

Organization

Country / Region

License

Feedback

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