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Titlebook: Drugs between Research and Regulations; Proceedings of the 5 C. Steichele (Medizinischer Direktor),U. Abshagen Conference proceedings 1985

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書目名稱Drugs between Research and Regulations
副標(biāo)題Proceedings of the 5
編輯C. Steichele (Medizinischer Direktor),U. Abshagen
視頻videohttp://file.papertrans.cn/284/283216/283216.mp4
圖書封面Titlebook: Drugs between Research and Regulations; Proceedings of the 5 C. Steichele (Medizinischer Direktor),U. Abshagen  Conference proceedings 1985
描述Franz Gross died suddenly during preparations for the meeting. He would have taken great pleasure in summarizing in this preface the aims and results of a gathering which so clearly bore his imprint as Chairman of the Scientific Program Committee. His sudden passing away is deeply regretted by all of us: organizers, speakers and participants. We greatly respect him for his exceptional abilities, his impact on science and his qualities as a human being. He provided the impulse for a well balanced and topical scientific program. We therefore dedicate the proceedings of this symposium to his memory. Munich was the fifth in a traditional line of international meetings of pharmaceutical physicians held at three-year intervals, starting in London in 1972 (‘International Aspects of Drug Evaluation and Usage‘), and followed by Florence in 1975 (,Rationality of Drug Development‘), Brussels in 1978 (,Pharmaceutical Medicine - the Future‘) and Paris in 1981 (‘Drug Safety -;- Progress and Controversies‘). This 5th meeting discussed improvements in drug development and application and examined the impact of regulatory activities.
出版日期Conference proceedings 1985
關(guān)鍵詞Rauwolfia; cancer; clinical trial; drug; drug development; drug safety; lipide; research; toxicity
版次1
doihttps://doi.org/10.1007/978-3-642-54130-8
isbn_softcover978-3-642-54132-2
isbn_ebook978-3-642-54130-8
copyrightSpringer-Verlag Berlin Heidelberg 1985
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els in 1978 (,Pharmaceutical Medicine - the Future‘) and Paris in 1981 (‘Drug Safety -;- Progress and Controversies‘). This 5th meeting discussed improvements in drug development and application and examined the impact of regulatory activities.978-3-642-54132-2978-3-642-54130-8
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The need of clinical drug trials in children be responsible for this “therapeutic orphan” situation of the child and these include the ignorance and indifference of drug manufacturers and pediatricians, a negative public attitude towards clinical research in general and an uncertainty in the legal and ethical requirements for drug testing in
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Outro,cceed, now and again, in thwarting their deliberations and obscuring their aims. The issue of Guidelines for the Clinical Investigation of Drugs is a case in point. They are hailed by some and condemned by others and nine tenths of the problem is that the one party really has little idea what the other party is talking about.
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