How to define limit for residual solvents in drug product

  Рет қаралды 7,615

Pharma Growth Hub

Pharma Growth Hub

Күн бұрын

Пікірлер: 12
@vinovishwa
@vinovishwa 3 жыл бұрын
Sir, you are great. It's very nice presentation also has more information. Thanks for doing this sir💐💐
@MohitKumarRohilla
@MohitKumarRohilla 6 ай бұрын
Nice explanation sir ... valuable information. Thank you so much
@krsraocreations9389
@krsraocreations9389 3 жыл бұрын
Good information sir thank u
@tanvirahmedsohag4086
@tanvirahmedsohag4086 3 жыл бұрын
Very good presentation, thanks
@ronnpawar1369
@ronnpawar1369 3 жыл бұрын
Gr8 explained. Please make a video on elemental impurity risk assessment as per ICHQ3d
@manojpotdar9516
@manojpotdar9516 2 жыл бұрын
very nicely explained
@mitaligaikwad1152
@mitaligaikwad1152 3 жыл бұрын
Very nicely explained. Request you to please share such informative video on calculation of elemental impurities as per ich q3d
@abhishekjoshi9650
@abhishekjoshi9650 Жыл бұрын
Very Useful
@TELINT-dp9vv
@TELINT-dp9vv 4 ай бұрын
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
@VijayKumar-ly2bl 2 жыл бұрын
Excellent ex
@Anvi2705
@Anvi2705 3 жыл бұрын
How to assign specification for Assay test
@NikitaBhiogade
@NikitaBhiogade 2 ай бұрын
Dear sir my solvent does not have PDE According to guidelines can i take 1.5ug/day for pde and convert it into mg/day And my MDD also in mg so do i need to convert it into grams ????
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