Contact details for Guideline SAHPGL-MD-03 Medical Device Vigilance: Adverse Events Reporting for License Holders

Name: Contact details for Guideline SAHPGL-MD-03 Medical Device Vigilance: Adverse Events Reporting for License Holders
Creator: South African Health Products Regulatory Authority
Keywords: adverse-events,communication,contacts,events,guidelines,industry,licenses,medical-devices,reporting,vigilance

Information

Original link

Type

Communication To Industry

Regulated products

Medical Devices

Published

July 9, 2024

Last updated

July 9, 2024

Description

Document Number MD01-2024/2025 - Version 1

Organization

South African Health Products Regulatory Authority (SAHPRA) 🇿🇦

Country / Region

South Africa

License

Other (Public Domain)

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1 Main file

Contact details for Guideline SAHPGL-MD-03 Medical Device Vigilance: Adverse Events Reporting for License Holders

Updated on July 9, 2024

pdf

URL: https://www.sahpra.org.za/wp-content/uploads/2024/07/Contacts-for-Adverse-Events-Recalls-and-Market-Actions_final.pdf
Permalink: https://data.openrid.co/en/datasets/r/11392b09-8285-4370-b8c1-afec1f915cab
MIME Type: application/pdf

Created on: July 9, 2024
Modified on: July 9, 2024

Contact details for Guideline SAHPGL-MD-03 Medical Device Vigilance: Adverse Events Reporting for License Holders

Information

Type

Regulated products

Published

Last updated

Description

Tags

Organization

Country / Region

License

Feedback

Actions

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