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Very informative video sir. Most of the pharmacy professional are unable to differentiate between them all. Going to show this video whenever they have a doubt
Sir I have one doubt, If a generic player is making one formulation, how they will get plasma concentration data (invivo) to correlate. Is invivo data generated by innovator available for public to correlate? Or generic players have to generate invivo data? Then it contradicts the bio waiver concept right? Please do reply
Please clarify my doubt For some BCS class 1 molecule with Tmax 1hr, dissolution media used is 6.8pH phosphate buffer Why don’t you select 1.2pH acid buffer by considering Tmax.
0.1 N HCl media 500 ml can and should be selected. If drug shows degradation in acid then other media can be selected. Other media use should be justified on scientific data.