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IMDRF/DITTA Joint Workshop on UDI was held on 9 September 2021

Unique Device Identifiers (UDIs) serve important regulatory and supply chain functions for medical devices. They allow for tracking of devices throughout the global supply chain to the patient and provide global visibility to device adverse event reporting and a better means to perform post-market surveillance, thereby enhancing patient safety.
10 September 2021

Member sites

Therapeutic Goods Administration

Brazilian Health Regulatory Agency (ANVISA)

Health Canada

National Medical Products Administration

European Commission Directorate-General for Internal Market, Industry, Entrepreneurship and SMEs

Pharmaceutical and Medical Devices Agency (PMDA)

Russian Ministry of Health

Health Sciences Authority

Ministry of Food and Drug Safety

Medicines and Healthcare products Regulatory Agency

US Food and Drug Administration

Regional harmonization initiatives

APEC LSIF Regulatory Harmonization Steering Committee

Global Harmonization Working Party (GHWP)

Pan American Health Organization (PAHO)

Official observers

Argentina, National Administration of Drugs, Food and Medical Devices

World Health Organization (WHO)

 

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