Dear All,
I am fairly new to R. I work mainly in SAS. Now, I know that SAS is approved
by the FDA for submissions. My question is, does the FDA approve {R} for
clinical trial submissions. Also has anyone ever tried to produce TFL's using
R. I would like to know how difficult it to produce the TFL's in R as compared
to SAS. I know that in SAS it is not difficult once you know what you are
doing
and what is required. My limited knowledge of R suggests that it may be a bit
more difficult. Can anyone please provide me with some guidance or sample code
for producing a standard table or listing. A good starting point can be a
demography table. I can produce a demog table quite easily in SAS. My R
knowledge is limited that's why I have ask for some sample code.
Thanks for your help.
Orin
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