Vol 10 No 3 (2022): VOLUME 10, ISSUE 3, 2022 | International Journal of Drug Regulatory Affairs

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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