How to carry out his clinical trial

Reference no: EM133291928

Question: Assume you are conducting the trial as the PI and using the KSU IRB. Complete the form using information you take from the Moderna protocol document. In the Moderna protocol, you will be able to find all of the information you need including but not limited to: the purpose, the aims, existing knowledge, the intervention, the participants, the data, etc. This manual of procedures document contains all of the information you will need to understand not only the IRB but how to carry out his clinical trial.

Reference no: EM133291928

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