Calling all ID's in pharmaceuticals - Clinical Trials
I'm working on a protocol deviation course and would like some ideas on how to make this course more engaging and interactive. If you can share some ideas or provide samples (if you can), I would be grateful.
Below are some of the objectives:
- Distinguish between important and non-important protocol deviations
- Describe the protocol deviation handling process
- Identify individual roles and responsibilities throughout the protocol deviation process
I'm not sure if I will be developing in Studio or Storyline at this point, so I will post this in the Storyline forum as well..
Thanks in advance.