- From: M. Scott Marshall <mscottmarshall@gmail.com>
- Date: Wed, 7 Jul 2010 12:10:52 -0700
- To: Susie Stephens <susie.stephens@gmail.com>
- Cc: public-semweb-lifesci hcls <public-semweb-lifesci@w3.org>
Hi Susie, Thanks for identifying this unique opportunity to engage with the FDA about data standards. I have re-pasted the URL's below for convenience because I had trouble accessing the versions in your previous message. I am printing the draft to locate specific issues where HCLS can contribute comments and suggestions. 1. Federal Register, 17 June 2010, 75(116), 34452-34453, http://edocket.access.gpo.gov/2010/pdf/2010-14637.pdf 2. FDA, CDER Data Standards Plan (Version 1.0), Posted online 17 June 2010, http://www.fda.gov/downloads/Drugs/DevelopmentApprovalProcess/FormsSubmissionRequirements/ElectronicSubmissions/UCM214120.pdf Cheers, Scott On Mon, Jul 5, 2010 at 11:28 AM, Susie Stephens <susie.stephens@gmail.com> wrote: > The FDA is announcing the availability for public comment of the draft > document entitled "CDER Data Standards Plan Version 1.0". The draft plan > outlines the general approach proposed for development of a comprehensive > data standards program in the Center for Drug Evaluation and Research > (CDER). The draft plan identifies key objectives for a data standards > program at CDER, processes to be developed to ensure successful use of those > standardized data, and a set of recommended projects beginning this calendar > year [1, 2]. > > Please let me know if you would be interested in contributing to > HCLS reviewing the plan and providing feedback. > > Cheers, > Susie > > > > 1. Federal Register, 17 June 2010, 75(116), 34452-34453, > http://edocket.access.gpo.gov/2010/pdf/2010-14637.pdf > > 2. FDA, CDER Data Standards Plan (Version 1.0), Posted online 17 June 2010, > www.fda.gov/downloads/Drugs/DevelopmentApprovalProcess/FormsSubmissionRequirements/ElectronicSubmissions/UCM214120.pdf
Received on Wednesday, 7 July 2010 19:11:22 UTC