International Journal of Drug Regulatory Affairs (IJDRA)

Table of Contents

• REVIEW ARTICLE

  Regulatory aspects for Biologic product licensing in India

  • Author: Sanjeev Kumar Maurya, Vikesh Shukla, Prachi Kaushik, SP Yamini Kanti, Anshul Bansal
  • DOI: 10.22270/ijdra.v7i1.287

• Filing of DMF in US, Canada & Europe

  • Author: S P Yamini Kanti, Neha Jain, Amrish Chandra, Vikesh Kumar Shukla
  • DOI: 10.22270/ijdra.v7i1.295

• A critical view of harmonization of regulatory requirements for Generic Drug approval submissions in ASEAN countries

  • Author: Jyoti Ghangas, Neha Jain, Anshuman Sinha
  • DOI: 10.22270/ijdra.v7i1.297

• Drug regulatory paradigm and challenges for Medical devices in India

  • Author: Anshul Bansal, Vikesh Kumar Shukla, Shikha Chauhan, Yamini Kanti SP, Sanjeev Kumar, Archita katrolia
  • DOI: 10.22270/ijdra.v7i1.299

• Drug approval process in India and Europe

  • Author: S P Yamini Kanti, Ildiko Csoka, Amrish Chandra, Vikesh Kumar Shukla
  • DOI: 10.22270/ijdra.v7i1.304

• Informed Consent form in Clinical Trial

  • Author: Sunny Panwar, Hemant Pal, Amrish Chandra
  • DOI: 10.22270/ijdra.v7i1.307

• Scenario of Over the Counter Medicines Worldwide

  • Author: Sunny Panwar, Khushboo Bhatia, Amrish Chandra
  • DOI: 10.22270/ijdra.v7i1.308

• Nanoparticles and target Drug delivery for cancer treatment: A Comprehensive review

  • Author: Nandish Pathak, Pratim Pathak
  • DOI: 10.22270/ijdra.v7i1.309