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Related Topic Tags
fda (food and drug administration), pharmaceuticals and pharmaceutical industry, 21 cfr part 820 - med. device mfger. qsr requirements, 21 cfr part 11 - electronic records and signatures, 21 cfr part 210 - cgmp for drugs, 21 cfr part 211 - finished pharmaceuticals cgmp, validation of machines equipment processes design etc., qualification of equipment and processes
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  #9  
Old 30th June 2009, 01:36 PM
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Re: New sub-forums within the FDA forum

Received. The moderators are starting to discuss. Give us 24 hours to discuss.
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  #10  
Old 1st July 2009, 02:05 PM
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Re: New sub-forums within the FDA forum

Quote:
In Reply to Parent Post by Juan Dude View Post

I just sent a report, my background is in medical devices, I have experience with validations, and I am qualified to, and would like to volunteer to help move threads.
As a heads up we're still discussing. The issue is mainly software user group permissions limitations.

I do want to tell you I very much appreciate the offer to help out. People in addition to you who may want to help out in different ways is one of the things that is on my mind. As the forum grows help is more and more appreciated and needed. At the same time I have to consider a number of potential aspects, including security aspects, of giving more people latitude to do things like move threads from forum to forum. As I say, there are software limitations, one of which is giving one set of permissions which are hard coded to include other permissions (i.e.: there are some 'all or nothing' settings).

Stay tuned!
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  #11  
Old 4th July 2009, 11:13 AM
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Re: New sub-forums within the FDA forum

Guys,

Give me few more days ... I shall move the threads
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  #12  
Old 12th October 2010, 02:00 AM
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Re: New sub-forums within the FDA forum

Quote:
In Reply to Parent Post by Ajit Basrur View Post

Hi all,

Based on the heavy response for Pharmaceutical related and other regulatory questions, we have created new sub forums within the FDA forum as follows -

Pharmaceuticals (21 CFR parts 210 & 211)

Medical Devices (21 CFR part 820)

Qualification and Validation (including 21 CFR Part 11)


Pl use these subforums for related questions and get more directed responses. The FDA forum itself can be used for 'General' questions or any other questions that doesnot fit in the subforums.

I, on behalf of all moderators take this oppurtunity in thanking the regular members and also the not so regular members for making the FDA section and the Cove so special
The changes have been made and this project has been completed. I should have noted it here some time ago.

Since the project was completed over a year ago I am closing this thread to new comments.
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