Materiovigilance

Author:

Soni Maneesh,Nandave Mukesh,Kumar Anoop

Publisher

Springer Nature Singapore

Reference17 articles.

1. CDSCO (2023) Central Drugs Standard Control Organization, Directorate General of Health Services Ministry of Health & Family Welfare Government of India. https://cdsco.gov.in/opencms/opencms/en/Medical-Device-Diagnostics/Medical-Device-Diagnostics/. Accessed 3 Oct 2023

2. Europa (2023) European Commission—EUDAMED. https://ec.europa.eu/health/md_eudamed/

3. FDA (2023) U.S. Food and Drug Administration (FDA)—postmarket requirements and commitments. https://www.fda.gov/medical-devices/postmarket-requirements-and-commitments

4. Health Canada (2023). Drug and medical device post market surveillance - Canada.ca. Accessed 2 Oct 2023

5. Joshi D, Sharma I, Gupta S, Singh TG, Dhiman S, Prashar A, Gulati M, Kumar B, Vishwas S, Chellappan DK, Gupta G (2021) A global comparison of implementation and effectiveness of materiovigilance program: overview of regulations. Environ Sci Pollut Res 28:1–22

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