International Journal Of Drug Regulatory Affairs

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

  • Author: Shrikant Godiyal
  • DOI: 10.22270/ijdra.v8i2.373

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

  • Author: Krishnasis Chakraborty
  • DOI: 10.22270/ijdra.v8i2.385

• Latest risk management guideline (iso 14971:2019) & environmental aspects of medical device

  • Author: Sunaina Mishra, Vikesh Kumar Shukla
  • DOI: 10.22270/ijdra.v8i2.387

• Indian Medical Device sector - blue print & regulatory policy roadmap

  • Author: Suchita Markan, Rajiv Nath, Jitendar Sharma, Dilip Kumar Chekuri
  • DOI: 10.22270/ijdra.v8i2.392

• Overview of drug regulatory affairs and drug approval process in US, Europe, India and Canada: A review

  • Author: Aishwarya Patil, Anjali Thakre
  • DOI: 10.22270/ijdra.v8i2.401

• Journey of Indian medtech sector from import dependence towards self-reliance: COVID-19 wakes-up the giant

  • Author: Suchita Markan, Rajiv Nath
  • DOI: 10.22270/ijdra.v8i2.403