RE: FDA documentation experience?

["Dan Goldstein" <DGoldstein -at- riverainmedical -dot- com>]

Medical device manufacturers can follow certain paper documentation
practices in order to avoid dealing with Part 11. However, Lin's
citation is relevant to them as well, since they have to know Part 11
well enough to stay outside its scope.

> -----Original Message-----
> From: Lin Sims
> Sent: Friday, September 05, 2008 10:37 PM
> To: 
> Cc: techwr-l -at- lists -dot- techwr-l -dot- com
> Subject: Re: FDA documentation experience?
> 
> Everything you need to know about FDA 21 CFR Part 11:
> 
> http://21cfrpart11.com/index.html
> 
> There are even free, recorded seminars/training.
> 

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