Background of the Study
Import and export regulations play a pivotal role in shaping the efficiency and cost-effectiveness of supply chains. In Nigeria’s pharmaceutical industry, compliance with regulatory requirements such as tariffs, licensing, and quality standards significantly impacts supply chain costs. While these regulations aim to ensure product safety and quality, they often increase operational expenses and lead to delays (Adetayo & Nwosu, 2024).
The pharmaceutical sector, heavily reliant on imported raw materials and finished products, is particularly vulnerable to changes in trade policies. This study examines how import and export regulations influence supply chain costs in Nigeria’s pharmaceutical industry, providing insights into strategies for cost optimization (Ifeanyi & Adeola, 2023).
Statement of the Problem
Stringent import and export regulations have become a significant cost driver for pharmaceutical companies in Nigeria. Compliance with these regulations often involves high tariffs, complex documentation, and prolonged approval processes, which delay supply chains and inflate costs. For an industry already grappling with economic challenges, these costs hinder competitiveness and accessibility to essential medicines (Okafor, 2023).
This study seeks to explore the effects of these regulations on supply chain costs and propose solutions for mitigating their impact while ensuring regulatory compliance.
Objectives of the Study
Research Questions
Research Hypotheses
Scope and Limitations of the Study
The study focuses on the Nigerian pharmaceutical industry, examining the period from 2023 to 2025. Limitations include potential difficulties in accessing comprehensive regulatory and financial data.
Definitions of Terms
Pharmaceutical Industry: The sector involved in the research, production, and distribution of medicines.
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