Bioequivalence and Bioavailability Forum

Dear Cap't'n,

» Is this an issue at all?

I think the risk of Mixing up is high when the PI and his/her clinical team are involved in both studies at the same time, think about adverse events which could be happened and his/her responsibility for the protection of study subjects, Mixing up in the collection of subjects study samples , ....etc


» In some countries the PI is purely an administrative matter; she or he will not see the subjects/patients but have everything delegated.

I know that in some very rare cases that the PI has purely an administrative job, but mostely he/she is a physician who do practically the clinical part from A to Z.

Best regards,
Osama