加勒比国家药监:一个概述
Kingsley E W Walker1, Reshma Bankay1, Satish Jankie2
1Department of Paraclinical Sciences, The University of the West Indies, St. Augustine, Trinidad and Tobago.
Current pharmacology reports
|June 26, 2023
概括
加勒比地区的药物监测系统需要得到显著的改进,才能达到世卫组织的标准. 越来越多的在线药品和伪造药品需要在整个地区改善营销后监测和不良药反应 (ADR) 报告.
科学领域:
- 制药科学 制药科学
- 公共卫生 公共卫生
- 监管事务 监管事务
背景情况:
- 随着COVID-19大流行,药品短缺加剧,在线获取药品的机会增加.
- 电子商务平台促进了低质量和伪造药品的广泛营销.
- 药品质量受到损害,需要加强制药行业的营销后监督.
研究的目的:
- 根据世卫组织的最低要求评估加勒比地区的药监系统.
- 强调光伏在确保加勒比地区药物安全方面的关键作用.
- 确定在该地区开发强大的光伏系统的挑战和机会.
主要方法:
- 在选定的加勒比国家对国家光伏系统的比较分析.
- 对遵守世卫组织药监指南的评估.
- 对药物不良反应 (ADRs) 的现有监管框架和报告机制的审查.
主要成果:
- 加勒比海的光伏系统在很大程度上不符合世卫组织的最低要求.
- 药物不良反应 (ADR) 报告是最小的,因为意识和参与度低.
- 很少有加勒比国家积极参与世卫组织全球光伏网络.
结论:
- 加勒比地区可持续的光伏系统需要立法和监管方面的改进.
- 加强政治承诺,资金和报告激励措施至关重要.
- 建设全面的光伏系统对于保护该地区的公共卫生至关重要.
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