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Vol 8 No 2 (2020): VOLUME 8, ISSUE 2, 2020
Review
Procedure to submit an Expression of Interest (EOI) for Product evaluation to Expert Review Panel (ERP) prequalification team: World Health Organization (WHO), Geneva
Shrikant Godiyal
Pages 1-6
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Abstract
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DOI
10.22270/ijdra.v8i2.373
DMF filing procedure in US, Europe and Canada: A Review
Krishnasis Chakraborty
Pages 7-14
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DOI
10.22270/ijdra.v8i2.385
Latest Risk Management guideline (ISO 14971:2019) & Environmental aspects of Medical Device
Sunaina Mishra, Vikesh Kumar Shukla
Pages 15-24
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DOI
10.22270/ijdra.v8i2.387
Indian Medical Device Sector - Blue Print & Regulatory Policy Roadmap
Suchita Markan, Rajiv Nath, Jitendar Sharma, Dilip Kumar Chekuri
Pages 25-35
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DOI
10.22270/ijdra.v8i2.392
Overview of Drug Regulatory Affairs and Drug approval process in US, Europe, India and Canada: A Review
Aishwarya Patil, Anjali Thakre
Pages 36-43
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DOI
10.22270/ijdra.v8i2.401
Journey of Indian Medtech Sector from Import Dependence towards Self-Reliance: COVID-19 wakes-up the Giant
Suchita Markan, Rajiv Nath
Pages 44-54
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DOI
10.22270/ijdra.v8i2.403
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Online ISSN: 2321-6794
Print ISSN: 2321-7162
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