Hi @Chris_Kirchberg
In the bio study, follwing are the steps that happen in sequence
1. selection of no. of volunteers
2. we give both the Innovator(Reference formulation) & the Test(generic) formulation to the volunteers
3. we then collect the blood, measure the concentration of the drug in the volunteers
4. This is followed by the geometric mean calculation of the Test and Reference
5. Finally, the Test/Reference ratio for the geomteric mean of the Test and reference is calculated.Regultory acceptance criertia is that the Test/Reference ratio along with the Confidence intervals should be in the range of 80-125 to conclude that there is no significant difference between the Reference and Test formulation
Selection of no. of volunteers is based on the power calculation, but i am not sure about the process/criteria that are involved. Kindly update me if this is possible with JMP.