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Vol 10 No 2 (2022): VOLUME 10, ISSUE 2, 2022
Research
Registration of health products for human use: Niger Republic case (from January 2018 to December 2020)
Mahaman Rabiou MAMANE IBRAHIM, Ousmane ABDOULAYE, Rakia ABDOU BAGOUGOU, Fatima GUIET MATI, Mahamadou OUDOU MOSSI MAIGA, Hamidou HAROUNA , Mahaman Laouali HAROUNA AMADOU, Kassoum JATAOU BAHARI , Nouhou HAMA AGHALI, Habsatou MINDAOUDOU, Bachir ILLO, Barira DAN NOUHOU
Pages 62-67
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Abstract
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DOI
10.22270/ijdra.v10i2.526
Clinical Trial Agreement – Eliminate legal problems when conducting clinical trials in Germany
Christoph Gerst, Christina Geringer, Thomas Voigt, Raees Ahmed
Pages 94-101
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DOI
10.22270/ijdra.v10i2.539
Review
A Comparison of the Drug Approval Process in the United States and Canada
Sylvia Botros, Mina Botros, Nancy Botros
Pages 1-8
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DOI
10.22270/ijdra.v10i2.514
A Comprehensive Study on Counterfeit Medicine and its prevention in India through its Regulatory Approach
Suryaprakash Singh, Priyanka Gupta
Pages 9-13
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DOI
10.22270/ijdra.v10i2.515
Assessment of Regulatory requirements and filing procedure of Drug Master File for Brazil, Europe and South Africa
Riya Patel, Kunal R. Girase, Venkateshwara T. Rao, Amit A. Patel, Ravish J. Patel
Pages 14-27
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DOI
10.22270/ijdra.v10i2.517
A Comparative Study of Biologic Regulation in US, Canada, Australia, Europe and Singapore
Yesha Patel, Amit A. Patel, Ravish J. Patel
Pages 28-34
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DOI
10.22270/ijdra.v10i2.518
Comparison of Dissolution profile for Immediate-Release Dosage form for US and Europe
Shivam Kanojiya, Neel Patel, Ravish J. Patel, Amit Patel
Pages 35-38
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DOI
10.22270/ijdra.v10i2.519
Regulatory perspective of Drug Repurposing: Methods, Regulatory pathways and Hurdles
Sonal Verma, Khushboo Vaghela, Maitreyi Zaveri
Pages 39-45
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DOI
10.22270/ijdra.v10i2.520
Analysis on the registration and review system of emergency medical devices in China and abroad in the context of COVID-19
Yiming Xu, Mingyang Wu, Wei Chen, Siyi Ge, Yi Liang
Pages 46-55
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DOI
10.22270/ijdra.v10i2.522
Bioequivalence requirements of Pharmaceutical Products in US, Europe and Australia
Nishi Patel, Jimesh Shah, Amit Patel, Ravish J. Patel
Pages 56-61
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DOI
10.22270/ijdra.v10i2.524
Regulations on Herbal Products in India, United States and European Union: A Review
Nirav Kumar Sapoliya, Mamta B Shah
Pages 67-72
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DOI
10.22270/ijdra.v10i2.528
AI models predicting Risk of Cardio Vascular Diseases - The Limitations, Challenges and Necessity for Regulatory Framework
Vyshnavi Belidhe, Suha Maryam, Srivani Siddala, Divya Chinthamalla, Chandrakanth Garela, Jithan Aukunuru Venkata, Vidya Sagar Jenugu
Pages 73-81
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DOI
10.22270/ijdra.v10i2.529
Strengthening Veterinary Pharmacy Regulations through the harmonization process in the UEMOA region: the case of Niger and Côte d'Ivoire
Fatima GUIET MATI, Sandra Wotsa VIDJRO, Kampadilemba OUOBA, Ramatou MOUMOUNI , Serge-Antoine AMARI, Jean-Yves PABST
Pages 82-89
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DOI
10.22270/ijdra.v10i2.533
Challenges and Future of Pharm D (Doctor of Pharmacy) Profession: Promising Career but with some reforms
Rishitha Kalchetty, Priyanka Lone, ChandiPriya Bonaboina, Sravani Rapher, LayaSree Panugantisira, Resika Kanukuntla, Ravi Kumar Badhavath, Madhusudhan Boddu, Jithan Aukunuru Venkata, Vidya Sagar Jenugu
Pages 90-93
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DOI
10.22270/ijdra.v10i2.535
Oncology Drugs: Evolution, Comparative study of Global Drug Regulatory approval process and various measures to improve availability and accessibility
Shagun Sharma, Khushbu Sharma, Pooja Verma, Shivali Rahi, Arpana Rana
Pages 102-111
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DOI
10.22270/ijdra.v10i2.542
Comparative Analysis of New Drugs and Clinical Trial Rules 2019 and its impact on Approval process of Oncology Drugs
Shagun Sharma, Khushbu Sharma, Pooja Verma, Shivali Rahi, Arpana Rana
Pages 112-130
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DOI
10.22270/ijdra.v10i2.543
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Online ISSN: 2321-6794
Print ISSN: 2321-7162
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