| Date: | Wed, 28 Nov 2007 21:14:19 -0500 |
| Reply-To: | SAS_learner <proccontents@GMAIL.COM> |
| Sender: | "SAS(r) Discussion" <SAS-L@LISTSERV.UGA.EDU> |
| From: | SAS_learner <proccontents@GMAIL.COM> |
| Subject: | Validation Process |
| Content-Type: | text/plain; charset=ISO-8859-1 |
Hell _all_ ,
I think this Topic must have discussed earlier as it is very old Topic We
are in Process of setting up validation Process for a Clinical submission,
I am looking for a paper or Place or any suggestions to Formally set a
validation Process. I know Most of the Pharmaceutical company's or the Big
CRO's they have Lot of Validated Macro's. Here we are Process of setting up
whole validation process from Scratch.
I am looking for some Place where there info about
1)Validation documents
2)Validation Procedures
Any books on validation Process which is acceptable by FDA. Thanks for all
the help
thanks
thanks
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