英国的无证药品——法律框架、风险及其管理

Ian M. Bourns
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引用次数: 4

摘要

英国制定有关药品许可的法律是为了减少使用药品造成伤害的可能性。无证药品不在危害管理程序之内;他们有额外的风险,需要复杂的专业责任。因此,药房实践采用的风险管理策略是专门针对如何管理无证药品的,特别是在使用无证药品风险最高的医院。由于不断增长的需求和成本——但资金不变——英国国民健康服务体系的医疗保健面临压力,正在经历一段转型和成本节约的时期。这种转变影响到药学实践和药品采购的所有领域。服务机构领导人需要在一段时期内(包括角色和职责的潜在变化)继续关注维持无证药品的安全系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unlicensed Medicines in the UK - Legal Frameworks, Risks, and their Management
The UK laws regarding the licensing of medicines have been developed to reduce the likelihood of harm through their use. Unlicensed medicines lie outside that harm management process; they have additional risks and require professional responsibilities that are complex. Therefore, pharmacy practice applies risk management tactics that are specific to how it manages unlicensed medicines, especially in hospitals, where the risks of their use is at its highest. Due to increasing demand and costs - but static funding - healthcare in the UK's National Health Service is under stress and undergoing a period of transformation and cost savings. That transformation affects all areas of pharmacy practice and medicines procurement. Service leaders need to keep a focus on maintaining safety systems for unlicensed medicines through a period of change, including potential changes in roles and responsibilities.
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