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