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pilot3.qmd
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pilot3.qmd
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---
title: "R Submission Pilot 3"
---
**Goals**:
- Expand on the work done in [Submission Pilot 1](pilot1.qmd), by now utilizing R to generate ADaM datasets.
- Deliver a publicly accessible R-based Submission to the FDA
**Key evaluation aspects**:
- For Submitter
- Generation of a reproducible R environment with a proprietary R package from git and open source R packages using `{renv}`
- Preparation of R-based submission materials
- For FDA Staff
- Reproduce analysis results by reproducing the R environment and retrieving both proprietary & open source packages
**Timeline**:
- Submitted to FDA on August 28th, 2023
- Feedback from FDA on February 2nd, 2024 (See feedback [here](https://rconsortium.github.io/submissions-wg/minutes/2024-02-02/))
- Re-submitted to FDA on April 19th, 2024
**Data and analysis scope**:
- ADaMs created using R (SDTM `.xpt` sourced from the CDISC Pilot study)
- TLFs created using R (ADaMs `.xpt` sourced from the ADaMs generated in R by the Pilot 3 team)
**Links**:
[R Submission Pilot 3 Development Repo](https://github.com/RConsortium/submissions-pilot3-adam)
- Development area for Pilot 3 Team
- See Closed Issues discussion for how we worked
- See [Wiki](https://github.com/RConsortium/submissions-pilot3-adam/wiki) for Common Issues we ran into and QC Findings we encountered when comparing the ADaMs generated in the CDISC Pilot study.
- We made use of a [GitHub Project Board](https://docs.github.com/en/issues/planning-and-tracking-with-projects/learning-about-projects/about-projects) (Kanban Style Board) to drive development.
[R Submission Pilot 3 eCTD Submission Package to FDA](https://github.com/RConsortium/submissions-pilot3-adam-to-fda)
- Materials submitted to the FDA following eCTD standards
[R Submission Pilot 3 Website](https://rconsortium.github.io/submissions-pilot3-adam/main/)
- Breakdown of the Github repositories and files used for analysis development, e-submission and proprietary Pilot 3 R Package
- Renderings of ADaMs, TLFs, ADRG and Cover Letter
- Discussions at Conferences and feedback from FDA
**Key team members**:
Developer team:
- Joel Laxamana-Roche
- Thomas Neitmann-Denali
- Phanikumar Tata-Syneos
- Robert Devine-J&J
- Steven Haesendonckx-J&J
- Lei Zhao-Roche
- Nicole Jones-Denali
- Kangjie Zhang-Bayer
- Benjamin Straub-GSK
- Declan Hodges-GSK
- Bingjun Wang - Merck
FDA Staff:
- Paul Schuette\
- Hye Soo Cho