Article(id=1322624505898447265, tenantId=1146029695717560320, journalId=1235980733773295621, issueId=1322624482217415197, articleNumber=null, orderNo=null, doi=10.20251/j.cnki.1003-3734.2026.19.001, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1785081600000, receivedDateStr=2026-07-27, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1793267855381, onlineDateStr=2026-10-29, pubDate=1791993600000, pubDateStr=2026-10-15, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1793267855381, onlineIssueDateStr=2026-10-29, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1793267855381, creator=13701087609, updateTime=1793267855381, updator=13701087609, issue=Issue{id=1322624482217415197, tenantId=1146029695717560320, journalId=1235980733773295621, year='2026', volume='35', issue='19', pageStart='2017', pageEnd='2128', issueExtLink='null', onlineDate='null', pubDate='1791993600000', pubDateStr='2026-10-15', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=1, specialIssue=null, createTime=1793267849735, creator='13701087609', updateTime=1793268229475, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1322626075042100008, tenantId=1146029695717560320, journalId=1235980733773295621, issueId=1322624482217415197, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1322626075046294313, tenantId=1146029695717560320, journalId=1235980733773295621, issueId=1322624482217415197, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=2017, endPage=2027, ext={EN=ArticleExt(id=1322624507219653026, articleId=1322624505898447265, tenantId=1146029695717560320, journalId=1235980733773295621, language=EN, title=Key changes and implementation considerations for 2026 version of Good Clinical Practice, columnId=null, journalTitle=Chinese Journal of New Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=
Objective:

To analyze the key changes in the 2026 edition of the good clinical practice (GCP) and to explore specific implementation measures.

Methods:

By interpreting the revised provisions of the new GCP edition and comparing them with the 2020 edition, together with reference to ICH E6 (R3), this study examines the implementation measures necessitated by these key changes.

Results:

The provisions regarding the management of trial protocols, investigator’s brochures, and essential documents, as well as most terminology, have been removed; implementation now follows ICH E6 (R3) guidelines, while retaining fundamental requirements and China-specific regulations. The General Provisions incorporate the three core principles of the ICH E6(R3), clarify the ultimate responsibilities of the principal investigator and the sponsor, introduce a separate chapter on data governance, and streamline the safety reporting process.

Conclusion:

To implement the new version of GCP and to promote the development of clinical drug trials in China, sponsors should align with international standards to strengthen their sense of responsibility and implement quality management and data governance; principal investigators and clinical trial institutions should enhance their awareness of ultimate responsibility and clarify the boundaries of authorization; and service providers should perform their duties in compliance with contractual obligations.

, authors=Xiao-ying YAO1, Song-tao CHEN2, Ji-yin ZHOU3, *, authorsList=Xiao-ying YAO, Song-tao CHEN, Ji-yin ZHOU, authorCompany=null, correspAuthors=Ji-yin ZHOU, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1322624507857187235, articleId=1322624505898447265, tenantId=1146029695717560320, journalId=1235980733773295621, language=CN, title=2026年版《药物临床试验质量管理规范》关键变化及落实思考, columnId=1322624486113915175, journalTitle=中国新药杂志, columnName=·2026年版《药物临床试验质量管理规范》解读专题, runingTitle=null, highlight=null, articleAbstract=
目的:

分析2026年版《药物临床试验质量管理规范》(Good Clinical Practice,GCP)的关键变化,思考落实的具体措施。

方法:

通过解读新版GCP修订条款及其与2020年版GCP的比较,结合ICH E6(R3)内容,探讨关键变化引发的落实措施。

结果:

删除试验方案、研究者手册和必备文件管理及大部分术语,具体参照E6(R3)执行,但保留原则性要求和中国特有规定;总则纳入E6(R3)三大核心理念,明确主要研究者和申办者的最终责任,新增数据治理独立章,理顺安全性报告流程。

结论:

为落实新版GCP以助推我国药物临床试验发展,申办者应当对接国际视野、加强责任意识,落实质量管理和数据治理,主要研究者和临床试验机构应增强最终责任意识、明确授权边界,服务供应商依合同合规落实。

, authors=姚晓颖1, 陈嵩涛2, 周吉银3, *, authorsList=姚晓颖, 陈嵩涛, 周吉银, authorCompany=null, correspAuthors=周吉银, authorNote=

姚晓颖,女,主任药师,主要从事药物临床试验机构管理。E-mail: 。

, correspAuthorsNote=

*

周吉银,男,博士研究生,副研究员,主要从事临床试验和医学伦理研究。 E-mail:。
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2026年版《药物临床试验质量管理规范》关键变化及落实思考
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姚晓颖 1 , 陈嵩涛 2 , 周吉银 3, *
中国新药杂志 | ·2026年版《药物临床试验质量管理规范》解读专题 2026,35(19): 2017-2027
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中国新药杂志 |·2026年版《药物临床试验质量管理规范》解读专题 2026 , 35 (19) : 2017 -2027
2026年版《药物临床试验质量管理规范》关键变化及落实思考
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姚晓颖1 , 陈嵩涛2, 周吉银3, *
作者信息
  • 1黑龙江省第三医院,哈尔滨 150046
  • 2拉萨市人民医院,拉萨 850000
  • 3陆军军医大学第二附属医院临床医学研究中心,重庆 400037
通讯作者:

*

周吉银,男,博士研究生,副研究员,主要从事临床试验和医学伦理研究。 E-mail:。
作者简介:

姚晓颖,女,主任药师,主要从事药物临床试验机构管理。E-mail: 。

Key changes and implementation considerations for 2026 version of Good Clinical Practice
Xiao-ying YAO1 , Song-tao CHEN2, Ji-yin ZHOU3, *
Affiliations
  • 1 The Third Hospital of Heilongjiang Province, Harbin 150046, China
  • 2 Lhasa People’s Hospital, Lhasa 850000, China
  • 3 Clinical Medical Research Center, Second Affiliated Hospital, Army Medical University, Chongqing 400037, China
出版时间: 2026-10-15 doi: 10.20251/j.cnki.1003-3734.2026.19.001
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目的:

分析2026年版《药物临床试验质量管理规范》(Good Clinical Practice,GCP)的关键变化,思考落实的具体措施。

方法:

通过解读新版GCP修订条款及其与2020年版GCP的比较,结合ICH E6(R3)内容,探讨关键变化引发的落实措施。

结果:

删除试验方案、研究者手册和必备文件管理及大部分术语,具体参照E6(R3)执行,但保留原则性要求和中国特有规定;总则纳入E6(R3)三大核心理念,明确主要研究者和申办者的最终责任,新增数据治理独立章,理顺安全性报告流程。

结论:

为落实新版GCP以助推我国药物临床试验发展,申办者应当对接国际视野、加强责任意识,落实质量管理和数据治理,主要研究者和临床试验机构应增强最终责任意识、明确授权边界,服务供应商依合同合规落实。

药物临床试验质量管理规范  /  ICH E6(R3)  /  关键变化  /  落实措施
Objective:

To analyze the key changes in the 2026 edition of the good clinical practice (GCP) and to explore specific implementation measures.

Methods:

By interpreting the revised provisions of the new GCP edition and comparing them with the 2020 edition, together with reference to ICH E6 (R3), this study examines the implementation measures necessitated by these key changes.

Results:

The provisions regarding the management of trial protocols, investigator’s brochures, and essential documents, as well as most terminology, have been removed; implementation now follows ICH E6 (R3) guidelines, while retaining fundamental requirements and China-specific regulations. The General Provisions incorporate the three core principles of the ICH E6(R3), clarify the ultimate responsibilities of the principal investigator and the sponsor, introduce a separate chapter on data governance, and streamline the safety reporting process.

Conclusion:

To implement the new version of GCP and to promote the development of clinical drug trials in China, sponsors should align with international standards to strengthen their sense of responsibility and implement quality management and data governance; principal investigators and clinical trial institutions should enhance their awareness of ultimate responsibility and clarify the boundaries of authorization; and service providers should perform their duties in compliance with contractual obligations.

Good Clinical Practice  /  ICH E6 (R3)  /  key changes  /  implementation measures
姚晓颖, 陈嵩涛, 周吉银. 2026年版《药物临床试验质量管理规范》关键变化及落实思考. 中国新药杂志, 2026 , 35 (19) : 2017 -2027 . DOI: 10.20251/j.cnki.1003-3734.2026.19.001
Xiao-ying YAO, Song-tao CHEN, Ji-yin ZHOU. Key changes and implementation considerations for 2026 version of Good Clinical Practice[J]. Chinese Journal of New Drugs, 2026 , 35 (19) : 2017 -2027 . DOI: 10.20251/j.cnki.1003-3734.2026.19.001
  • 陆军军医大学人文社会科学基金重点资助项目(2022XRW02)
参考文献 引证文献
排序方式:
[1]
张亚美, 何芹, 周吉银. ICH《E6(R3):药物临床试验质量管理规范技术指导原则》变化亮点和主要修订内容[J]. 中国医学伦理学, 2026, 39(5): 557-564.
[2]
王白璐, 张静. 浅谈ICH E6 R(3)的主要变更及其对药物临床研发行业的影响[J]. 中国临床药理学杂志, 2025, 41(16): 2351-2356.
[3]
江柯萱, 周吉银. 2024年版《赫尔辛基宣言》的重大变化及实施思考[J]. 中国医学伦理学, 2025, 38(4): 403-411.
[4]
周吉银. 2020年版《药物临床试验质量管理规范》研究者和申办者保护受试者的要求[J]. 中国医学伦理学, 2021, 34(2): 205-210.
[5]
卜丽娟, 江柯萱, 周吉银. 去中心化临床试验的挑战、对策及伦理审查要点[J]. 中国医学伦理学, 2024, 37(4): 399-407.
[6]
罗嵇宁, 陈一飞, 徐瑛. 关于申办者的药物临床试验质量管理体系建设的探讨[J]. 上海医药, 2021, 42(13): 6-9.
2026年第35卷第19期
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doi: 10.20251/j.cnki.1003-3734.2026.19.001
  • 接收时间:2026-07-27
  • 首发时间:2026-10-29
  • 出版时间:2026-10-15
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  • 收稿日期:2026-07-27
基金
陆军军医大学人文社会科学基金重点资助项目(2022XRW02)
作者信息
    1黑龙江省第三医院,哈尔滨 150046
    2拉萨市人民医院,拉萨 850000
    3陆军军医大学第二附属医院临床医学研究中心,重庆 400037

通讯作者:

*

周吉银,男,博士研究生,副研究员,主要从事临床试验和医学伦理研究。 E-mail:。
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小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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