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  1. Home /
  2. Archives /
  3. 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
    • View PDF Abstract Download PDF DOI 10.22270/ijdra.v8i2.373
  • DMF filing procedure in US, Europe and Canada: A Review
    Krishnasis Chakraborty
    Pages 7-14
    • View PDF Abstract Download PDF 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
    • View PDF Abstract Download PDF 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
    • View PDF Abstract Download PDF 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
    • View PDF Abstract Download PDF 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
    • View PDF Abstract Download PDF DOI 10.22270/ijdra.v8i2.403
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Online ISSN: 2321-6794
Print ISSN: 2321-7162
CODEN (CAS-USA): IJDRAF





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