Quality and regulation standards for positron emission tomography equipment and bone marrow cell separator as medical devices in India

Author:

Walia Ramanpreet,Pandey Nidhi,Jain GauravKumar,Thakkar ArtiR

Publisher

Medknow

Subject

General Pharmacology, Toxicology and Pharmaceutics

Reference14 articles.

1. Sector Survey: Medical Devices; 2020. Available from: https://www.makeinindia.com/article/-/v/sector-survey-medical-devices. [Last accessed on 2020 Sep 17].

2. CDSCO Official Website. Available from: https://cdsco.gov.in/opencms/opencms/en/Home/. [Last accessed on 2018 Jul 18].

3. Drug Controller General of India, Directorate General of Health Services, FDA Bhawan; Classification of Newly Notified Medical Devices. Available from: https://cdsco.gov.in/opencms/opencms/en/Medical-Device-Diagnostics/Medical-Device-Diagnostics/. [Last accessed on 2020 Dec 17].

4. Health Ministry Notifies Medical Devices Rules 2017. Press Information Bureau, Government of India; 2017. Available from: https://cdsco.gov.in/opencms/export/sites/CDSCO_WEB/Pdf-documents/medical-device/digosfaq19.pdf. [Last accessed on 2018 Aug 28].

5. European Commission. Guidelines for the Classification of Medical Devices; 2001. Available from: https://tinyurl.com/y7ccb9bl. [Last accessed on 2019 Jul 18].

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