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紅蜻蜓好運(yùn)銀蟲 (著名寫手)
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[求助]
IRB approval or waiver statement in the Materials and Methods section. 已有2人參與
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Include IRB approval or waiver statement in the Materials and Methods section. The Clinical Trial Registration number, if applicable, should be included at the end of the abstract. sci投稿,讓校稿。編輯發(fā)了這個(gè),什么意思?是需要加什么說明嗎?麻煩蟲友指點(diǎn),多謝。 發(fā)自小木蟲Android客戶端 |
銀蟲 (著名寫手)
新蟲 (小有名氣)
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臨床試驗(yàn)需要倫理文員會(huì)的批準(zhǔn)文件,你需要在method部分提供論文的試驗(yàn)獲得所在機(jī)構(gòu)倫理委員會(huì)的聲明,可以的話在摘要末尾附上臨床試驗(yàn)的注冊(cè)編號(hào) 發(fā)自小木蟲Android客戶端 |
新蟲 (小有名氣)
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*獲得所在機(jī)構(gòu)倫理委員會(huì)批準(zhǔn)的聲明 順便住題主新春快樂,萬事如意 發(fā)自小木蟲Android客戶端 |
銀蟲 (著名寫手)
超級(jí)版主 (文學(xué)泰斗)
No gains, no pains.
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專家經(jīng)驗(yàn): +21105 |
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Institutional Review Board (IRB): An independent body constituted of medical, scientific, and non-scientific members, whose responsibility is to ensure the protection of the rights, safety and well-being of human subjects involved in a trial by, among other things, reviewing, approving, and providing continuing review of trial protocol and amendments and of the methods and material to be used in obtaining and documenting informed consent of the trial subjects. 倫理委員會(huì),一般為獨(dú)立倫理委員會(huì):指由醫(yī)學(xué)、藥學(xué)及其他背景人員組成的委員會(huì),其職責(zé)是通過獨(dú)立地審查、同意、跟蹤審查試驗(yàn)方案及相關(guān)文件、獲得和記錄受試者知情同意所用的方法和材料等,確保受試者的權(quán)益、安全受到保護(hù)。 |
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