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Titlebook: Cancer Policy: Pharmaceutical Safety; June M. McKoy,Dennis P. West Book 2019 Springer Nature Switzerland AG 2019 Drug Safety.Health.Oncolo

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發(fā)表于 2025-3-21 19:27:19 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書(shū)目名稱(chēng)Cancer Policy: Pharmaceutical Safety
編輯June M. McKoy,Dennis P. West
視頻videohttp://file.papertrans.cn/222/221175/221175.mp4
概述Describes the latest thoughts and findings relating to drug safety in the cancer domain.Covers emerging strategies to identify adverse drug reactions and drug-drug interactions.Highlights policies ins
叢書(shū)名稱(chēng)Cancer Treatment and Research
圖書(shū)封面Titlebook: Cancer Policy: Pharmaceutical Safety;  June M. McKoy,Dennis P. West Book 2019 Springer Nature Switzerland AG 2019 Drug Safety.Health.Oncolo
描述Cancer Policy: Pharmaceutical Safety provides invaluable information on the interesting and compelling field of cancer drug safety. Identifying and understanding high-priority policy issues and key pharmacovigilance strategies is of paramount importance. In this volume, outstanding and original chapters provide an overview and synthesis of the latest thoughts and findings relating to drug safety in the cancer domain. Topics include natural language processing and pharmacovigilance of alternative cancer pharmaceuticals. The information presented in this volume will improve understanding of emerging strategies to identify adverse drug reactions and drug-drug interactions within the cancer setting and will highlight policies that have been instituted to improve cancer patient safety. In summary, Cancer Policy: Pharmaceutical Safety explores many of the important areas of pharmacovigilance research in oncology.
出版日期Book 2019
關(guān)鍵詞Drug Safety; Health; Oncology; Pharmaceutical; Policy; Toxicity
版次1
doihttps://doi.org/10.1007/978-3-319-43896-2
isbn_ebook978-3-319-43896-2Series ISSN 0927-3042 Series E-ISSN 2509-8497
issn_series 0927-3042
copyrightSpringer Nature Switzerland AG 2019
The information of publication is updating

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New Documentaries in Latin AmericaThis Chapter provides an introduction and overview of the U.S. FDA REMS program and applicable regulatory aspects. Topics covered include the 2015 Draft Guidance, organization structure and functions, a discussion on pharmacovigilance and adverse event reports, and a discussion of the applicability of REMS in oncology.
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June M. McKoy,Dennis P. WestDescribes the latest thoughts and findings relating to drug safety in the cancer domain.Covers emerging strategies to identify adverse drug reactions and drug-drug interactions.Highlights policies ins
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Essay 2: Environmental Performance,ic concerns drive drug safety improvements. This chapter examines pressures on drug costs due to the complexity of care and drug therapies, marked structure in which care is provided, and regulatory requirements driving safety.
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