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首页> 外文期刊>Journal of Pharmacological and Toxicological Methods >The Diplomate in Safety Pharmacology (DSP) certification scheme
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The Diplomate in Safety Pharmacology (DSP) certification scheme

机译:安全药理学文凭课程(DSP)

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摘要

As with other professional disciplines there is a growing need from within industry as well as global regulatory authorities for implementation of a certification process in order to assure that appropriate expertise is developed and quality standards are identified for professionals involved in the practice of Safety Pharmacology (SP). In order to meet this need, the Safety Pharmacology Society (SPS) has developed the Diplomate in Safety Pharmacology (DSP) certification process. There are many benefits to certification including authentication of the discipline within the overall pharmaceutical community and with regulatory authorities. It also encourages participation in SPS activities by other professionals (toxicologists, clinicians, academics) who wish to broaden their professional expertise. It provides an opportunity for candidates to strengthen their fundamental scientific knowledge, and stimulates the sharing of data, methods and model development in the form of publications and presentations on relevant topics in SP. Accreditation in SP occurs after candidates successfully complete a written certification examination conducted at the annual SPS meeting. The DSP exam consists primarily of material pertinent to the conduct of SP vital function core battery studies (i.e., cardiovascular, respiratory and central nervous systems), supplemental SP studies (i.e., renal/urinary, gastrointestinal, immunology, and hematology), Regulatory Guidelines (ICH Guidelines) as well as relevant cross-functional knowledge (e.g., physiology, pharmacology, toxicology, biochemistry, pathology, pharmacokinetics, dosing formulation, analytical methods, and statistics). Maintenance of the DSP certification results from the accrual of credits which are gained from a range of educational and scientific contributions. Eligibility requirements include a combination of at least a bachelor degree in science and two years of relevant professional SP experience and one poster presentation on a SP topic as first author at a recognized major scientific meeting. (C) 2015 Elsevier Inc. All rights reserved.
机译:与其他专业学科一样,行业以及全球监管机构也越来越需要实施认证过程,以确保开发出适当的专业知识并为参与安全药理学(SP)实践的专业人员确定质量标准。 )。为了满足此需求,安全药理学会(SPS)已开发了安全药理学(DSP)文凭课程。认证有很多好处,包括在整个制药界和监管机构对学科进行认证。它还鼓励希望扩展其专业知识的其他专业人员(毒理学家,临床医生,学者)参加SPS活动。它为候选人提供了增强其基础科学知识的机会,并通过以SP的相关主题为主题的出版物和演示形式来促进数据,方法和模型开发的共享。候选人成功完成在SPS年度会议上进行的书面认证考试后,即可进行SP认证。 DSP考试主要由与SP重要功能核心电池研究(即心血管,呼吸系统和中枢神经系统),补充性SP研究(即肾/泌尿,胃肠道,免疫学和血液学)相关的材料,监管指南组成(ICH指南)以及相关的跨职能知识(例如,生理学,药理学,毒理学,生物化学,病理学,药代动力学,剂量配方,分析方法和统计数据)。 DSP认证的保持是通过累积学分而产生的,这些学分是通过一系列教育和科学贡献而获得的。资格要求包括至少具有科学学士学位和两年相关SP专业经验,以及在公认的重大科学会议上作为第一作者的SP主题海报演示。 (C)2015 Elsevier Inc.保留所有权利。

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