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Medical Device Clinical Evaluation Standard Operating Procedure / SOP

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Posted 29th May 2016 at 01:53 PM by sherley13

Dear All,

Recent ISO 13485 Auditors has been asking for Post Market Surveillance procedure ( SOP)/for Medical devices if you have anyone please share with us.

Thank you.

sherley 13
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  1. Old Comment
    Marc's Avatar
    You might want to post his in a forum because this is the Blog section of Elsmar. You will probably get better response(s) in a forum post by starting a new discussion thread there.

    This might be a good forum to post in: http://elsmar.com/Forums/forumdisplay.php?f=16
    Posted 31st May 2016 at 12:11 PM by Marc Marc is online now
 
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