question relating to trials, page-6

  1. 961 Posts.
    Yep- nothing quatitative in regards to FDA approval.
    But, everything else in regards to good business practice is.
    Dolph expresses the same thing that bitter old me has continually stated- CCE stuffed their trial protocols to a level that warrants genuine criticism.

    At least dolphin didn't give a time period of completion. This would be full of crud - how can you predict how many applicable burn victims in a certain time?

    But- find out how many patients required!
    And
    how many are completed

 
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