https://github.com/RConsortium/rtrs-wg
The R Consortium working group, R Tables for Regulatory Submissions (RTRS) includes representation from several large pharmaceutical companies and CRO’s. The goal of the working group is to create standards for creating tables that meet the requirements of FDA submission documents, and hence enhance the suitability of R for FDA submissions. It is part of a larger R Consortium effort to facilitate the certification and validation of R packages and tools for FDA submissions thereby allowing drug developers to submit documentation for regulatory approval using the R programming environment in conjunction with open-source packages without the need for closed and often expensive proprietary tools.
Let's talk about working group goals, work in progress, challenges and ideas in discussions. It's a great place to ask questions about buiding tables and documents for clinical trial submissions, discuss some ideas, engage with others, and much more!
Please feel free to file an issue. From gt (special character encoding in RTF): https://github.com/rstudio/gt/blob/bae32f432f190a904e26c3d1396b63ea65e5106a/R/utils_render_rtf_redo.R#L536