The lingo here is not just about semantics.
Trials “start” when the first patient is consented.
If you start a trial prior to registering it - it will not be prospective.
If you start a trial prior to IRB approval you will be in the doo doo.
Engaging a CRO and talking to potential sites are preparatory activities prior to starting a trial. So basically preparatory activities are "underway".
The lingo here is not just about semantics. Trials “start” when...
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