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...issues usually come up when discussing the use of R for FDA trials: 1. Most FDA submissions come down to a series of r x k tables, and it is hard to claim that one system is better than another for that. 2. Data is to be submitted to the FDA in SAS (considered by many as the industry standard) or CDISC XML formats (http://www.cdisc.org/); there are pretty good SAS tools for that; does R have comparable? 3. Some packages in R provide acknowledgedly better functionality than their SAS-equivalent, but an entire FDA validation would have to occur each time an enhancement is made to the R package be...

I see in the archives significant discussion about SAS, CDISC formats etc. for FDA, but no direct suggestion of adding a write.xport method to the foreign package. Are there significant barriers to doing so? [[alternative HTML version deleted]]

Hi all there Can some one clarify me on this issue, features wise which is better R or SAS, leaving the commerical aspect associated with it. I suppose there are few people who have worked on both R and SAS and wish they would be able to help me in deciding on this. THank you for the help --------------------------------- [[alternative HTML version deleted]]