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Consultation closed

Patient Registry: Essential Principles

Start date

Saturday, 16 January 2016

Closing date

Saturday, 16 January 2016

Working group

Integrating patient registries and innovative tools for enhanced medical device evaluation and tracking

Consultation documents

Please use the comments template to provide comments on this document.

xls (56.5 KB)

Member sites

Therapeutic Goods Administration

Brazilian Health Regulatory Agency (ANVISA)

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)