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Vol 7 No 1 (2019): VOLUME 7, ISSUE 1, 2019
Review
Nanoparticles and target Drug delivery for cancer treatment: A Comprehensive review
Nandish Pathak, Pratim Pathak
Pages 53-58
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Abstract
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DOI
10.22270/ijdra.v7i1.309
Regulatory aspects for Biologic product licensing in India
Sanjeev Kumar Maurya, Vikesh Shukla, Prachi Kaushik, SP Yamini Kanti, Anshul Bansal
Pages 1-5
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DOI
10.22270/ijdra.v7i1.287
Filing of DMF in US, Canada & Europe
S P Yamini Kanti, Neha Jain, Amrish Chandra, Vikesh Kumar Shukla
Pages 6-12
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DOI
10.22270/ijdra.v7i1.295
Drug regulatory paradigm and challenges for Medical devices in India
Anshul Bansal, Vikesh Kumar Shukla, Shikha Chauhan, Yamini Kanti SP, Sanjeev Kumar, Archita katrolia
Pages 25-33
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DOI
10.22270/ijdra.v7i1.299
Drug approval process in India and Europe
S P Yamini Kanti, Ildiko Csoka, Amrish Chandra, Vikesh Kumar Shukla
Pages 34-40
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DOI
10.22270/ijdra.v7i1.304
Informed Consent form in Clinical Trial
Sunny Panwar, Hemant Pal, Amrish Chandra
Pages 41-46
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DOI
10.22270/ijdra.v7i1.307
Scenario of Over the Counter Medicines Worldwide
Sunny Panwar, Khushboo Bhatia, Amrish Chandra
Pages 47-52
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DOI
10.22270/ijdra.v7i1.308
A critical view of harmonization of regulatory requirements for Generic Drug approval submissions in ASEAN countries
Jyoti Ghangas, Neha Jain, Anshuman Sinha
Pages 13-24
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DOI
10.22270/ijdra.v7i1.297
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Online ISSN: 2321-6794
Print ISSN: 2321-7162
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