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  1. Home /
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  3. Vol 10 No 3 (2022): VOLUME 10, ISSUE 3, 2022

Research

  • Regulatory Compliance of Small-Scale Pharmaceutical manufacturing facilities in Addis Ababa, Ethiopia
    Wondue Ketele, Tesfa Marew, Motlalepula Matsabisa, Gebremariam Birhanu
    Pages 1-9
    • View PDF Abstract Download PDF DOI 10.22270/ijdra.v10i3.540
  • Evaluation of the Patentability of Medicines based on plants produced in Cameroon: Case of Yaounde
    Minyem Ngombi Afuh Aude Périne, Ekeme Kevin, Maniepi Saurelle, Soppo Lobe Vanessa Charlotte, Nyangono Ndongo Martin, Mbole Mvondo Jeanne Mauricette, Benga Chimène, Nnanga Nga
    Pages 19-24
    • View PDF Abstract Download PDF DOI 10.22270/ijdra.v10i3.547
  • Real World studies on undesirable effects of some Anti-Thrombotic Drugs in a tertiary Hospital
    Meghna Mehta, Vidya Sagar
    Pages 42-53
    • View PDF Abstract Download PDF DOI 10.22270/ijdra.v10i3.552
  • Agreements for the financial or material support of a non-commercial clinical trial in Germany
    Raees Ahmed, Theresa Möller, Matthias Siegert
    Pages 25-31
    • View PDF Abstract Download PDF DOI 10.22270/ijdra.v10i3.550

Review

  • FDA Regulatory Implications for Co-crystals and recent Co-crystal Patents
    Samuel Rigilin, Krishnananda Kamath Kunjal, Abdul Raheem Thayyil, Ramakrishna Shabaraya
    Pages 10-18
    • View PDF Abstract Download PDF DOI 10.22270/ijdra.v10i3.541
  • Product Life Cycle Management in Europe: A Review
    Krishnasis Chakraborty, Ravichandra V D
    Pages 32-41
    • View PDF Abstract Download PDF DOI 10.22270/ijdra.v10i3.551
  • The Enlightenment of the Management of EU Notified Bodies to China's Introduction of Third-Party Institutions for Medical Device Supervision
    Qingqing Hou, Yiming Xu, Dawei Zhang, Yi Liang
    Pages 54-60
    • View PDF Abstract Download PDF DOI 10.22270/ijdra.v10i3.553
  • Comparison of Dietary Supplements Product Registration requirements in Singapore, Malaysia, Ghana, Zimbabwe and India
    Ritu Kakadia, Utsav Patel, Maitreyi Zaveri, Vinit Movaliya, Khushboo Vaghela, Niranjan Kanki
    Pages 61-65
    • View PDF Abstract Download PDF DOI 10.22270/ijdra.v10i3.531
  • Regulatory requirement for the approval of Generic Drug in Vietnam as per ASEAN Common Technical Dossier (ACTD)
    Vruddhi Panchal, Utsav Patel, Vinit Movaliya, Khushboo Vaghela, Niranjan Kanki, Maitreyi Zaveri
    Pages 66-69
    • View PDF Abstract Download PDF DOI 10.22270/ijdra.v10i3.532
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Online ISSN: 2321-6794
Print ISSN: 2321-7162
CODEN (CAS-USA): IJDRAF





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