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282 * ! Wed, 8/11/2021, 1:30 PM - 3:20 PM Virtual
Tools to Enable the Use of R by the Biopharmaceutical Industry in a Regulatory Setting — Topic-Contributed Papers
Biopharmaceutical Section
Organizer(s): Marly Gotti, Biogen; Juliane Manitz, EMD Serono
Chair(s): Juliane Manitz, EMD Serono
1:35 PM A Risk-Based Approach for Assessing R Package Accuracy Within a Validated Infrastructure
Paulo Bargo, Janssen R&D; Juliane Manitz, EMD Serono; Andy Nicholls, GSK; Doug Kelkhoff, Roche; Yilong Zhang, Merck & Co., Inc.; Lyn Taylor , Phastar; Joe Rickert, R Consortium; Marly Gotti, Biogen; Keaven M Andersen, Merck & Co. Inc.
1:55 PM riskmetric: A Risk-based Workflow to Evaluate the Quality of R Packages
Doug Kelkhoff, Roche
2:15 PM Paving the Way for Regulatory Submissions Using R: the Risk Assessment Shiny Application
Marly Gotti, Biogen
2:35 PM Packages for Automated Assessment and Standards Alignment of R Packages
Mark Padgham, rOpenSci; Noam Ross, Ecohealth Alliance
2:55 PM R2rtf - A Lightweight R Package to Produce Submission-Ready Tables and Figures in RTF Format
Yilong Zhang, Merck & Co., Inc.; Siruo Wang, John Hopkins University; Simiao Ye, Merck & Co., Inc.; Madhusudhan Ginnaram, Merck & Co., Inc.; Keaven M Andersen, Merck & Co. Inc.
3:15 PM Floor Discussion