How to define limit for residual solvents in drug product

[@MohitKumarRohilla]

Nice explanation sir ... valuable information. Thank you so much

[@vinovishwa]

Sir, you are great. It's very nice presentation also has more information.
Thanks for doing this sir💐💐

[@krsraocreations9389]

Good information sir thank u

[@mitaligaikwad1152]

Very nicely explained. Request you to please share such informative video on calculation of elemental impurities as per ich q3d

[@ronnpawar1369]

Gr8 explained. Please make a video on elemental impurity risk assessment as per ICHQ3d

[@manojpotdar9516]

very nicely explained

[@tanvirahmedsohag4086]

Very good presentation, thanks

[@TELINT-dp9vv]

It is said that api and excipient 2 does not meet option 2, but it meets option 2 not the option 1, see video 14:03 to 14:12 min. Now please clarify should we compare api and excipient 2 to option 1 or 2?

[@VijayKumar-ly2bl]

Excellent ex

[@abhishekjoshi9650]

Very Useful

[@Anvi2705]

How to assign specification for Assay test