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11 articles for “NDA”
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First Insights into Whole Genome Sequencing of the Mycobacterium tuberculosis Complex: Molecular Diversity and Drug Susceptibility Patterns in Senegal
Abstract: Background: We conducted a bibliographic analysis of the Mycobacterium tuberculosis complex (MTBC) in sub-Saharan Africa, which included the analysis of 8,139 genomic sequences from 34 of the 49 sub-Saharan African countries. Notably, only one complete sequence from Senegal was identified, which had been generated in the United States. Our primary objective was to utilize whole genome sequencing (WGS) to detect resistance in anti-tuberculous strains of the MTBC in Senegal. This …
Published in Recent Trends in Infectious Diseases · Vol. 2, Issue 1, 2025 · pp. 1–14 Read article
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Live Epidemiological Tracking of COVID-19 in Senegalese Participants of the Hajj
Abstract: Background: Since the COVID-19 outbreak, global efforts have focused on controlling the disease. However, intense cross border movements pose a risk for the emergence of new SARS-CoV-2 strains. A recent example is the detection of cases among the 2024 Senegalese pilgrims returning from Mecca, Saudi Arabia. Investigations of these cases have revealed genomic evolution of the virus. The lack of surveillance may lead to the emergence of high-threat strains. This …
Published in Recent Trends in Infectious Diseases · Vol. 2, Issue 2, 2025 · pp. 8–16 Read article
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Petroleum and The Nigerian Economy (1999–2007): Between NEO-Colonialism and Domestic Collaborators
Abstract: This paper analyzes the state of the petroleum sector and its impact on Nigerian economy from 1999–2007. The manner in which the sector was managed attracted a wide range of comments on the rationale for the administration’s handling of the petroleum industry. Between 1999 and 2007, President Obasanjo’s Government failed to reposition the Nigerian oil sector in such a way that it will benefit all Nigerians. Instead, the administration opened …
Published in Journal of Offshore Structure and Technology · Vol. 1, Issue 2, 2014 · pp. 8–14 Read article
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Land Appropriation in Shonga Community in Nigeria: The Zimbabwe Farmers Connection
Abstract: This paper seeks to examine the impact of the invitation of Zimbabwe white commercial farmers in changing the land ownership patterns and breeding tension in Shonga community of Kwara state, Nigeria. The objective of the paper is to highlight the effects of land appropriation by the state in favour of the Zimbabwe white farmers, and which has contributed to the revolt by the local farmers against the new order. The …
Published in OmniScience: A Multi-disciplinary Journal · Vol. 4, Issue 2, 2014 · pp. 26–30 Read article
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Nigeria-Zimbabwe Bilateral Relations: Issues and Challenges
Abstract: Nigeria-Zimbabwe bilateral relations were struck in the early 1980s when Zimbabwe attained political independence during the administration of Alhaji Shehu Shagari. The diplomatic relations between the two countries were warm and cordial in the period 1980–2004. The objective of this paper is to examine the issues that have resulted to the low ebb in Nigeria-Zimbabwe bilateral relations in recent years. Secondary data were utilized in this paper. Books, Journals, magazines …
Published in OmniScience: A Multi-disciplinary Journal · Vol. 4, Issue 2, 2014 · pp. 31–35 Read article
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Regulatory Requirements for Pharmaceutical Product Registration in UAE
Abstract: Over the past decade, the healthcare industry in the United Arab Emirates (UAE) has experienced remarkable growth, positioning itself as the second-largest healthcare industry in the Middle East, trailing only Saudi Arabia. Recognizing the significance of healthcare, the UAE government has prioritized its development and actively promoted it as part of the national development plan. The Ministry of Health (MOH) has played a crucial role in this endeavor by allocating …
Published in Research & Reviews: A Journal of Drug Formulation, Development and Production · Vol. 11, Issue 1, 2024 · pp. 1–7 Read article
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Clinical Trials: A Brief Review
Abstract: Clinical trials, according to the World Health Organization, are used to test new medicinal entities on humans after they have been studied in animals. Clinical studies are usually divided into five stages. Clinical pharmacologists study phase I pharmacokinetics, safety, and gross effects on human volunteers. If the drug passes the test, it moves on to phase II testing, where pharmacokinetics, safety, and therapeutic efficiency are studied on a small number …
Published in Research & Reviews: A Journal of Drug Design & Discovery · Vol. 9, Issue 1, 2022 · pp. 1–7 Read article
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A Brief Note on Different Concept of Biowaiver
Abstract: The aim of the present work was to understand the concept of to waive a complete and systemic bioequivalence (BE) study. Biowaiver or request for a biowaiver is a fast track approach to boost the drug development process. Over the past three-four years, the biowaiver market has shown greater number of biowaiver submissions and the wider use of in-vitro permeability study. Biowaiver is a beneficial approach for getting approval of …
Published in Research & Reviews: A Journal of Drug Formulation, Development and Production · Vol. 3, Issue 3, 2016 · pp. 22–30 Read article
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Progressive collapse analysis study of rc building:a review
Abstract: The progressive collapse of building is that the collapse of whole building or a part of building in progressive manner thanks to spread of local failure from element to element. thanks to progressive collapse there'll be severe loss of building and lifetime of humanity as progressive collapse happens suddenly. Toavoid the loss got to design a building by proper study and analysis of building for progressive collapse. thanks to earthquake, …
Published in Recent Trends in Civil Engineering & Technology · Vol. 11, Issue 2, 2021 · pp. 13–19 Read article
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Drug Product Registration in US, EUROPE, JAPAN and CANADA for New Drug and Generics
Abstract: Getting a marketing approval includes various junctures such as getting drug substances from approved vendors, finished product development, clinical studies, plant inspection, dossier writing and finally submission to authorities. US, Europe, Japan and Canada are the countries which are regulated for the approval of pharmaceutical products. These countries follow the ICH guidelines for the registration of drug of drug product. But each country has different type of application for the …
Published in Research & Reviews: A Journal of Drug Formulation, Development and Production · Vol. 1, Issue 3, 2014 · pp. 1–7 Read article
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Drug Master File—Electronic Submission through eCTD: An Overview
Abstract: A Drug Master File (DMF) is a supporting document for various applications such as Investigational New Drug Application (IND), New Drug Application (NDA), Abbreviated New Drug Application (ANDA), Biologic License Application (BLA), etc. Mainly product’s chemistry, manufacturing, and control (CMC) part is covered in the DMF. As per the current guidelines of US Food & Drug Administration (USFDA), all types of DMFs are mandatory to be submitted through Electronic Common …
Published in Trends in Drug Delivery · Vol. 6, Issue 1, 2019 · pp. 8–13 Read article