Implementation of adverse event reporting for medical devices, India-Reference-Cited by-同舟云学术

Implementation of adverse event reporting for medical devices, India

Published:2019-11-18 Issue:3 Volume:98 Page:206-211
ISSN:0042-9686
Container-title:Bulletin of the World Health Organization
language:
Short-container-title:Bull. World Health Organ.

Author:

Shukla Shatrunajay¹,Gupta Madhur²,Pandit Sabitri¹,Thomson Milu¹,Shivhare Abhimanyu¹,Kalaiselvan Vivekanandan¹,Singh Gyanendra Nath³

Affiliation:

1. Medical Device & Materiovigilance Programme of India, Indian Pharmacopoeia Commission, Ministry of Health & Family Welfare, Government of India, Sector-23, Raj Nagar, Ghaziabad-201002, Uttar Pradesh, India.

2. Office of the WHO Representative to India, New Delhi, India.

3. Indian Pharmacopoeia Commission, Ministry of Health & Family Welfare, Uttar Pradesh, India.

Publisher

WHO Press

Subject

Public Health, Environmental and Occupational Health

Reference7 articles.

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3. Woman who sued Johnson & Johnson for faulty implant dead [internet]. The Times of India. 2014 May 12. Available from: https://timesofindia.indiatimes.com/city/mumbai/Woman-who-sued-Johnson-Johnson-for-faulty-implant-dead/articleshow/34986373.cms [cited 2019 Nov 6].

4. Indian regulatory update: January–December 2017.;Bhave;Perspect Clin Res,2018

5. Medical device regulations: a current perspective.;Gupta;J Young Pharm,2016

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