显示页面修订记录反向链接回到顶部 修订记录 以下是当前文档的修订记录。如果要回复到某个旧的修订版,请在下面选择它,并点击“编辑本页”,之后保存即可。 2022/02/18 08:49 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) 老T +102 B (当前版本) 2022/02/18 08:38 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [D. “适用的临床试验(Applicable Clinical Trials)”的知情同意要素] 老T +15 B 2022/02/18 08:35 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [A. 知情同意的一般要求] 老T +4 B 2022/02/18 05:58 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [E.知情同意文件] 老T -2 B 2022/02/18 05:54 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [H. 中止/终止研究] 老T +19 B 2022/02/18 05:53 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [H. 中止/终止研究] 老T +3 B 2022/02/18 05:53 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [G. 受试者参与一项以上临床研究] 老T +3 B 2022/02/18 05:53 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [F. 儿童受试者] 老T +3 B 2022/02/18 05:49 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [F. 儿童受试者] 老T -1 B 2022/02/18 05:49 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [F. 儿童受试者] 老T -15 B 2022/02/18 05:48 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [F. 儿童受试者] 老T -3 B 2022/02/18 05:46 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [D. FDA] 老T -7 B 2022/02/18 05:40 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [B. 临床研究者] 老T +36 B 2022/02/18 05:39 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [D. FDA] 老T +72 B 2022/02/18 05:37 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [A. 患者记录的审阅] 老T +35 B 2022/02/18 05:34 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [C. 申办者] 老T +72 B 2022/02/18 05:32 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [B. 临床研究者] 老T -4 B 2022/02/18 05:31 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [A: IRB] 老T -20 B 2022/02/18 05:28 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [E.知情同意文件] 老T +116 B 2022/02/18 05:26 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [B. 知情同意的基本要素] 老T -4 B 2022/02/18 05:25 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [B. 知情同意的基本要素] 老T +187 B 2022/02/18 04:37 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [A. 知情同意的一般要求] 老T +6 B 2022/02/18 04:34 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [A: IRB] 老T +3 B 2022/02/18 04:34 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [E.知情同意文件] 老T +153 B 2022/02/18 04:32 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [E.知情同意文件] 老T +193 B 2022/02/18 04:28 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [C. 知情同意的其他要素] 老T +609 B 2022/02/18 04:25 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [B. 知情同意的基本要素] 老T +789 B 2022/02/18 04:19 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [A. 知情同意的一般要求] 老T +74 B 2022/02/18 04:17 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [A. 患者记录的审阅] 老T +92 B 2022/02/18 04:14 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [E.知情同意文件] 老T +90 B 2022/02/18 04:12 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [D. “适用的临床试验(Applicable Clinical Trials)”的知情同意要素] 老T +22 B 2022/02/18 04:12 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [C. 知情同意的其他要素] 老T -3 B 2022/02/18 04:11 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [C. 知情同意的其他要素] 老T +160 B 2022/02/18 04:10 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [B. 知情同意的基本要素] 老T +69 B 2022/02/18 04:09 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [B. 知情同意的基本要素] 老T +138 B 2022/02/18 04:07 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [A. 知情同意的一般要求] 老T ±0 B 2022/02/18 04:06 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [A. 知情同意的一般要求] 老T ±0 B 2022/02/18 04:06 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [A. 知情同意的一般要求] 老T ±0 B 2022/02/18 04:05 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [A. 知情同意的一般要求] 老T +23 B 2022/02/18 04:05 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [II. “知情同意过程”概述] 老T +55 B 2022/02/18 04:03 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [I. 介绍] 老T +94 B 2022/02/18 04:02 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) 老T -38 B 2022/02/18 03:55 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [I. 介绍] 老T +65 B 2022/02/17 19:05 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [D. “适用的临床试验(Applicable Clinical Trials)”的知情同意要素] 老T -3 B 2022/02/17 18:11 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [A. 知情同意的一般要求] 老T ±0 B 2022/02/17 17:10 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [F. 儿童受试者] 老T +336 B 2022/02/17 15:28 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [C. 读写及计算能力较低的受试者] 老T +8 B 2022/02/17 15:28 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [C. 读写及计算能力较低的受试者] 老T +282 B 2022/02/17 14:22 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [B. 不会讲英语的受试者] 老T +6 B 2022/02/17 14:22 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [B. 不会讲英语的受试者] 老T -41 B 2022/02/17 14:09 知情同意指南(Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors) – [C. 读写及计算能力较低的受试者] 老T -5 B 显示跟目前版本的差异 较旧的 >> 法规/知情同意指南.txt 最后更改: 2年前由 老T