T/CGCPU 025-2023 Clinical CRO Activity Guideline
T/CGCPU 025-2023 Clinical CRO Activity Guideline
Basic Information
Scope
Main technical content: Foreword Introduction 1 Scope 2 Normative reference documents 3 Terms and definitions, abbreviations 3.1 Terms and definitions 3.2 Abbreviations 4 Evaluation content 4.1 Clinical trial protocol design 4.2 Selection of clinical trial institutions and principal investigators 4.3 Clinical trial implementation process 4.4 Clinical trial monitoring 4.5 Risk-based monitoring/centralized monitoring 4.6 Clinical trial audits 4.7 Drug safety and pharmacovigilance 4.8 Clinical trial management 4.9 Protection of subjects' rights 4.10 Financial management 5 Evaluation content details 6 Evaluation conclusion determination principles Appendix A (normative) Evaluation content details Appendix B (informative) Clinical CRO evaluation content References