| Regulatory Deliverables |
| These documents below are referenced in the FDA Study Data Technical Conformance Guide (click here to view FDA Study Data Standards Resources). These are also referenced in the PMDA Technical Conformance Guide on Electronic Study Data Submissions (click here to view PMDA New Drug Review with Electronic Data). |
Integrated Analysis Data Reviewer’s Guide (iADRG) Package Version 1.0, 18 September 2023 | The cSDRG and ADRG apply to a single study. Sponsors have used these templates when creating a reviewer's guide for integrated Study Data and reviewer's guide for integrated Analysis Data. The template has to be changed in order to document the information for multiple studies. |
Bio-research Monitoring Data Reviewers Guide (BDRG) Package Version 3.0, 28 June 2023 | The BDRG provides regulatory agency reviewers an orientation to the submitted Bioresearch Monitoring (BIMO) data in a consistent way and usable format. The BDRG Package includes Introduction and Overview, Template, Completion Guidelines and Examples. |
Nonclinical Study Data Reviewer's Guide (nSDRG) Package Version 1.2 08 April 2022 | The nSDRG provides regulatory agency reviewers with additional context for nonclinical tabulation datasets received as part of a regulatory submission. The nSDRG Package includes the template and completion guidelines. |
Analysis Data Reviewer's Guide (ADRG) Package Version 1.2, 18 July 2019 | The ADRG provides regulatory agency reviewers an orientation to the submitted analysis data in a consistent way and usable format. This Package includes information on the Legacy Data Conversion Plan and Report (LDCP) appendix. The ADRG Package includes the template, completion guidelines, and examples. |
Version 1.3, 2 November 2018 | The cSDRG provides regulatory agency reviewers an orientation to the submitted tabulation data in a consistent way and usable format. This Package includes information on the Legacy Data Conversion Plan and Report (LDCP) appendix. The cSDRG Package includes the template, completion guidelines, examples, and example traceability diagrams. |
Study Data Standardisation Plan (SDSP) Package Version 1.0, 16 January 2018 | The SDSP documents the data standardisation approach for clinical and nonclinical studies within a development program. This Package includes information on the CBER appendix, with proposed domain/variable usage. The SDSP Package includes the template, completion guidelines, sponsor implementation guide, and examples. |
If you wish to view the extensive list of all PHUSE published deliverables, click here. |