当前位置:首页 >英文主页 >中英对照 > 中译版报告详情

EFPIA & CRA:2024年创新药物不可及和延迟上市的根本原因分析报告(中译版)(41页).pdf

上传人: Y**** 编号:175012 2024-09-18 41页 2.70MB

下载:

1、The root causes of unavailability of innovative medicines and delays in access June 2024 Page 1 The root causes of unavailability of innovative medicines and delay in access:Shortening the wait Executive Summary1 The unprecedented speed of innovation exhibited over the last five years and the promis

2、e of the industry pipeline2 provide an important opportunity to improve outcomes for patients.There is common agreement that the value of innovation is realised only when patients benefit from advances in treatment.However,a significant number of medicines are not available across all European Union

3、(EU)markets.3 EFPIA has for many years looked at the length of time it takes for medicines to be made available.As illustrated by the most recent data in the Patient W.A.I.T.Indicator Survey in 2023,the average time to reimbursement for innovative treatments across EU and European Economic Area coun

4、tries has reached 531 days,ranging from 126 days in Germany to 990 days in Turkey.4 There are patient access inequities within Europe,with significant differences across countries in the number of products available at any given time and that the time taken prior to national reimbursement also varie

5、s significantly from one country to another.The industry shares concern about these delays and recognise that delays and the unavailability of medicines harm patients.These concerns are important context for the debate regarding the impact of the EUs General Pharmaceutical Legislation and whether it

6、 will improve access to medicines for patients in the EU.Over the past four years,EFPIA has documented the root causes of access inequality and found 10 interrelated factors that explain unavailability and delay(defined as length of time from European marketing authorisation to availability at the m

word格式文档无特别注明外均可编辑修改,预览文件经过压缩,下载原文更清晰!
三个皮匠报告文库所有资源均是客户上传分享,仅供网友学习交流,未经上传用户书面授权,请勿作商用。
本文主要讨论了创新药物在欧洲联盟(EU)成员国之间可获得性和延迟的原因。文章指出,创新药物的价值只有在患者从治疗进步中受益时才能实现。然而,许多药物在所有欧盟市场都不可用。文章分析了导致创新药物不可用和延迟的10个相互关联的因素,包括缓慢的监管过程、市场准入评估的延迟启动、重复的证据要求、报销延迟和本地配方决策。文章还指出,这些根本原因可以通过利益相关者共同努力解决。 文章提供了关于创新药物在欧洲不同国家之间可获得性差异的数据。例如,2023年患者等待指标调查显示,欧盟和欧洲经济区国家创新治疗的平均报销时间为531天,从德国的126天到土耳其的990天不等。文章还指出,随着时间的推移,欧洲各地创新药物的延迟逐渐增加。 文章强调,为了提高患者对创新药物的可及性并减少欧洲各国之间的不平等,需要多利益相关者合作,并考虑根本原因的多元性。欧洲制药工业协会(EFPIA)及其成员已经制定了一系列具体提案,以提高患者对创新药物的可及性并减少欧洲各国之间的不平等。
创新药物在欧洲的可用性如何? 欧洲药品审批延迟的原因是什么? 如何解决欧洲药品审批延迟问题?
客服
商务合作
小程序
服务号
折叠