Calling all pharma ID's - Clinical Trials

Hi all,

I am in the process of designing/developing a course on protocol deviation (process change). I would love to see what others are doing in this area.  Any ideas for making this dry topic more engaging and interactive? Here are a few of the learning objectives for your information:

  • Distinguish between important and non-important protocol deviations
  • Describe the protocol deviation handling process
  • Identity individual roles and responsibilities throughout the protocol deviaton process

Thanks in advance.


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