Draft-广东省生物统计学会

17 2023.03

Guidance on the Design and Protocol Development of Real-World Studies for Drugs (Draft)

01 2021.11

Guideline on Integrated Summary of Efficacy for Clinical Trials (Draft)

25 2021.04

Guideline on Enrichment Strategies and Designs in Clinical Trials (Draft)

01 2020.11

Guideline on Adaptive Designs for Clinical Trials（Draft）

01 2020.11

Guideline on Non-inferiority Clinical Trials (Draft)

01 2020.11

Guideline on Clinical Trial Data Monitoring Committees(Draft)

01 2020.11

Guideline on the Submission of Clinical Trial Data (Draft )

01 2020.11

Key Considerations in Using Real-World Evidence to Support Drug Development (Draft)

01 2020.11

Guidance on Using Real-World Data to Generate Real-World Evidence (Draft)