Use of RWE to Inform Regulatory, Public Health Policy, and Intervention Priorities for the Developing World

干预(咨询) 公共卫生 发展中国家 业务 公共卫生政策 监管科学 卫生政策 公共经济学 环境卫生 环境规划 医学 经济增长 经济 环境科学 护理部 病理
作者
Douglas McNair,Murray Lumpkin,Steven E. Kern,Daniel Hartman
出处
期刊:Clinical Pharmacology & Therapeutics [Wiley]
卷期号:111 (1): 44-51 被引量:21
标识
DOI:10.1002/cpt.2449
摘要

For low‐ and middle‐income countries (LMICs) to benefit from real‐world evidence (RWE)/real‐world data (RWD) in both product registration (“regulatory”) decision making and in product utilization policy (“policy”) decision making, they need to overcome several challenges. They need to deploy more electronic health records systems (EHRs), adjust for confounder variables, build trust between stakeholders, and create laws and regulations for local generation of data that are assented for secondary use. The role of procurers and their use of RWE/RWD in the LMIC context likewise is in a state of ongoing development. Procurers of health products are strong players currently in the “access” chain as LMICs continue to work on strengthening governmental health technology assessment (HTA) bodies. Procurers’ use of RWE is presently at an early stage and is mostly indirect, leveraging RWE results that are produced by researchers in high‐income countries (HICs), often under considerably different regulatory and policy objectives and constraints compared to LMICs’ epidemiology and priorities. Pending wider deployment of EHRs and other RWE sources, stakeholders must realize that populations from HIC RWE (i) can be devised to closely resemble phenotypic patterns in LMIC populations and (ii) can be analyzed to align with LMICs’ unmet needs.

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