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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• DMF filing procedure in US, Europe and Canada: A Review

  Krishnasis Chakraborty

  Pages 7-14

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• Latest Risk Management guideline (ISO 14971:2019) & Environmental aspects of Medical Device

  Sunaina Mishra, Vikesh Kumar Shukla

  Pages 15-24

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• 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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• 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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• 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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