Calling all pharma ID's - Clinical Trials
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.