如何改善对翻新医疗器械的监管实践
Shatrunajay Shukla1, Vivekanandan Kalaiselvan1, Rajeev Singh Raghuvanshi1
1Indian Pharmacopoeia Commission, Ministry of Health & Family Welfare, Government of India, Sector-23, Raj Nagar, Ghaziabad-201002, Uttar Pradesh, India.
Bulletin of the World Health Organization
|June 2, 2023
概括
全球对翻新医疗器械的需求正在上升,特别是在资源较低的国家. 制定明确的国际法规对于确保这些基本医疗保健工具的质量和安全至关重要.
科学领域:
- 生物医学工程 生物医学工程
- 卫生政策 卫生政策
- 医疗器械规则 医疗器械规则
背景情况:
- 医疗保健机构越来越依赖医疗器械.
- 快速的技术进步使得购买新设备具有挑战性,特别是在资源较少的环境中.
- 这导致全球对翻新医疗器械的需求日益增长,特别是在低收入和中等收入国家.
研究的目的:
- 分析全球主要市场对翻新医疗器械的监管环境.
- 确定医疗器械装修行业的机遇和挑战.
- 倡导标准化的监管准则,以确保设备的质量和安全.
主要方法:
- 对重装医疗器械现行法规的比较分析.关键国家.
- 探索市场趋势,机遇和挑战.
- 对恢复医疗设备的安全和性能标准的审查.
主要成果:
- 在国际上,管理翻新医疗器械的法规存在显著差异.
- 新的医疗设备有严格的规定,与他们的翻新对手不同.
- 翻新设备市场为医疗保健提供了机会和挑战.
结论:
- 需要对翻新医疗器械的进口,销售,标签和使用制定标准化的监管准则.
- 当局实施这些指南对于保持高质量和安全标准至关重要.
- 解决监管漏洞将提高全球医疗保健系统中翻新医疗设备的可用性和可靠性.
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