A comparative study of medical device regulation between countries based on their economies
Document Type
Article
Publication Title
Expert Review of Medical Devices
Abstract
Introduction: Medical devices play a crucial role in healthcare, addressing the diagnosis, treatment, and monitoring of various medical conditions. This study conducts a comprehensive analysis of medical device regulations across nations, considering the economic contexts of diverse countries. Areas Covered: The research involves a comparative examination of medical device regulations, dissecting unique frameworks in countries like the United States (US), European Union (EU), India, and Africa. These nations were chosen based on economic significance, market influence, and regulatory structures. The study aims to achieve a nuanced understanding of global medical device regulation, develop strategies to enhance guidelines, especially in developing nations, and provide recommendations for improvements in relevant regions. Expert Opinion: Through this study, valuable insights are gained into the diverse regulatory frameworks governing medical devices globally. The analysis identifies areas within these frameworks that require improvement, as well as strategies to enhance regulatory guidelines, particularly addressing the specific needs of developing economies. Ultimately, the research provides significant recommendations for policymakers and industry stakeholders. By offering a deeper understanding of regulatory intricacies, this study establishes pragmatic approaches to address challenges within the medical device industry and improve the regulatory landscape on a global scale.
First Page
467
Last Page
478
DOI
10.1080/17434440.2024.2360979
Publication Date
1-1-2024
Recommended Citation
Chettri, Bijaya and Ravi, Ramya, "A comparative study of medical device regulation between countries based on their economies" (2024). Open Access archive. 10973.
https://impressions.manipal.edu/open-access-archive/10973
