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International Journal Of Drug Regulatory Affairs
Year 2020, Volume-8, Issue-2 (June)
Print ISSN : 2321-2162
Online ISSN : 2321-6794 Table of contents Review Article 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 DMF filing procedure in US, Europe and Canada: A review
Krishnasis Chakraborty Latest risk management guideline (iso 14971:2019) & environmental aspects of medical device
Sunaina Mishra, Vikesh Kumar Shukla Indian Medical Device sector - blue print & regulatory policy roadmap
Suchita Markan, Rajiv Nath, Jitendar Sharma, Dilip Kumar Chekuri Overview of drug regulatory affairs and drug approval process in US, Europe, India and Canada: A review
Aishwarya Patil, Anjali Thakre Journey of Indian medtech sector from import dependence towards self-reliance: COVID-19 wakes-up the giant
Suchita Markan, Rajiv Nath Top |
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