提示! 期刊投稿指南社区正式上线内测,尚有很多功能并未实现,如果您在测试过程中发现期刊信息有错误,请戳此反馈:期刊信息问题。网站功能问题,请加站长微信:620100690
  1. 首页
  2. 英文期刊PHARMACOLOGY & PHARMACY

PHARMACOEPIDEMIOLOGY AND DRUG SAFETY

PHARMACOEPIDEM DR S

ISSN:1053-8569 E-ISSN:1099-1557  出版商:Wiley  国家:ENGLAND  周期:Bimonthly

影响因子(2024)
2.400
中科院分区(2025 官方末版)
3 区
JCR 分区
Q2
审稿周期
约13 周
录用比例
75.00%
收录情况  h-index:85  CiteScore:4.40
投稿入口: 投稿系统  期刊官网 

期刊简介

The aim of Pharmacoepidemiology and Drug Safety is to provide an international forum for the communication and evaluation of data| methods and opinion in the discipline of pharmacoepidemiology. The Journal publishes peer-reviewed reports of original research| invited reviews and a variety of guest editorials and commentaries embracing scientific| medical| statistical| legal and economic aspects of pharmacoepidemiology and post-marketing surveillance of drug safety. Appropriate material in these categories may also be considered for publication as a Brief Report. Particular areas of interest include: design| analysis| results| and interpretation of studies looking at the benefit or safety of specific pharmaceuticals| biologics| or medical devices| including studies in pharmacovigilance| postmarketing surveillance| pharmacoeconomics| patient safety| molecular pharmacoepidemiology| or any other study within the broad field of pharmacoepidemiology; comparative effectiveness research relating to pharmaceuticals| biologics| and medical devices. Comparative effectiveness research is the generation and synthesis of evidence that compares the benefits and harms of alternative methods to prevent| diagnose| treat| and monitor a clinical condition| as these methods are truly used in the real world; methodologic contributions of relevance to pharmacoepidemiology| whether original contributions| reviews of existing methods| or tutorials for how to apply the methods of pharmacoepidemiology; assessments of harm versus benefit in drug therapy; patterns of drug utilization; relationships between pharmacoepidemiology and the formulation and interpretation of regulatory guidelines; evaluations of risk management plans and programmes relating to pharmaceuticals| biologics and medical devices.

投稿经验(0 条,)

数据整理自公开网络的投稿反馈,仅供参考。