5 WHYS | WHY WHY | SIMPLIFIED!
17:30
Q2(R2): Performance Characteristic
32:41
Capsule Shell: History & Size
7:33
QA vs QC | PHARMA JOBS
12:00
11 ай бұрын
Пікірлер
@AnkitYadav-lg9zs
@AnkitYadav-lg9zs Күн бұрын
Sir please make separate playlist for this
@jihadnajib1369
@jihadnajib1369 Күн бұрын
Please explain us analytical development
@SudhakarPanchal-e8l
@SudhakarPanchal-e8l 2 күн бұрын
For A 266
@SudhakarPanchal-e8l
@SudhakarPanchal-e8l 2 күн бұрын
266
@deedeedirac5350
@deedeedirac5350 2 күн бұрын
Hola, me encantó el video muchas gracias, podrías compartirme la hoja de Excel por favor, gracias
@rajugopale4651
@rajugopale4651 2 күн бұрын
Nice information. Surfactant use in tier 2 also need to cover in this presentation sir.
@rukhsar581
@rukhsar581 4 күн бұрын
Very nice video
@ramachandrarana7751
@ramachandrarana7751 4 күн бұрын
Very good information
@piyu9853
@piyu9853 6 күн бұрын
Thanks !!
@krish_krish354
@krish_krish354 12 күн бұрын
Mass balance anywhere mentioned 95_105 limit in anvisa where i have to check
@AmitRaj-yr5ry
@AmitRaj-yr5ry 12 күн бұрын
Very informative sir🙏
@Fgffhjhfrgghhh
@Fgffhjhfrgghhh 12 күн бұрын
Nice explanation ❤
@Hawk-eye-i
@Hawk-eye-i 12 күн бұрын
Sir, why don’t we go first calibration due date with PQ approval date, it makes sense that the instrument is intended for Use only after PQ approval. So next calibration due will be set based on the PQ approval date. Correct me if am wrong. What are the risk associated with this approach?
@jayprakashmittal3870
@jayprakashmittal3870 14 күн бұрын
Wrong weighing Pipetting Dilution also obvious error
@ankitthackar9154
@ankitthackar9154 17 күн бұрын
Very helpful video sir thank you
@tannaprasanthkumar2356
@tannaprasanthkumar2356 17 күн бұрын
Tnq sir nice voice
@rahulm4068
@rahulm4068 17 күн бұрын
Very Informative sir, Giving explanation with Example that’s makes us easy understanding. That’s makes you different from others, I have seen plenty of videos they just read the content that’s all. No explanation 😊 I Hope in future you will make more videos on such topics
@mamatapanthi6987
@mamatapanthi6987 18 күн бұрын
Sir One class is needed for excel for this calculationa.In maximum cases regulatory body excels are locked.So calculation formula for excel highly needed
@rahulm4068
@rahulm4068 18 күн бұрын
Very Informative video. sir plz make detail video on ICHQ14, Thank you 😊
@blazedelif
@blazedelif 20 күн бұрын
queen allah mı buda mı artık tanrın neyse razı olsun beynimiz çıktı sunu öğrencez die
@vivekrajkotia3730
@vivekrajkotia3730 21 күн бұрын
❤ awesome
@4fourty242
@4fourty242 21 күн бұрын
Good explanation sir
@FaresAlZamn
@FaresAlZamn 22 күн бұрын
Thank you for the good detailed explanation
@prabhashsharma7938
@prabhashsharma7938 24 күн бұрын
Do we need to use 3 batches for performing Analytical method validation?
@pharmagrowthhub3083
@pharmagrowthhub3083 23 күн бұрын
only one batch
@prabhashsharma7938
@prabhashsharma7938 21 күн бұрын
@@pharmagrowthhub3083 ​ Thanks sir for prompt response Somewhere i read following and CFT staff also suggested the following "In the case of new method which is non-pharmacopeial three consecutive batches to be validated in AMV to prove the method is correct to analyze the sample" In case of Process validation i had always used 3 batches multiple times but in case of AMV i have considertd only one batch (Since last 14 years) . Are 3 batches required for any specific market (Finished product) as my current organisation is using the 3 batches from quite sometime.
@prabhashsharma7938
@prabhashsharma7938 24 күн бұрын
Do we need to use 3 batches for performing Analytical method validation?
@pharmagrowthhub3083
@pharmagrowthhub3083 22 күн бұрын
only one batch
@prabhashsharma7938
@prabhashsharma7938 24 күн бұрын
Do we need to use 3 batches for performing Analytical method validation?
@prabhashsharma7938
@prabhashsharma7938 24 күн бұрын
Do we need to use 3 batches for performing Analytical method validation?
@prabhashsharma7938
@prabhashsharma7938 24 күн бұрын
Do we need to use 3 batches for performing Analytical method validation?
@arunabhasanyal2252
@arunabhasanyal2252 25 күн бұрын
Extremely helpful. Thank you sir
@kalpanayarram3289
@kalpanayarram3289 25 күн бұрын
Thank you soo much sir
@abdullahalajrame5689
@abdullahalajrame5689 26 күн бұрын
when you will give
@BETCOREENGINEERINGBETcore
@BETCOREENGINEERINGBETcore 27 күн бұрын
Please how can I have S/N directly on report from empower
@kishorjadhav931
@kishorjadhav931 27 күн бұрын
Excellent
@vivekrajkotia3730
@vivekrajkotia3730 29 күн бұрын
Simply awesome 🙌
@maheshgupta564
@maheshgupta564 29 күн бұрын
Can you provide protocol pdf
@Pramod-m3y4v
@Pramod-m3y4v 29 күн бұрын
Thanks sir for nice technical presentation.It will very helpful for all pharma professional during method development
@shashikantnandanikar5388
@shashikantnandanikar5388 Ай бұрын
Thanks for information session. Well understood. In one of our project of Tablets one known impurity is increasing Initial (0 day) it was 0.12% 6M acc condition 1.8% All unknown impuriites are well within control
@sriv2013
@sriv2013 Ай бұрын
May I know the difference between remedial action, inter action and correction?
@avinashkale7916
@avinashkale7916 Ай бұрын
Excellent
@hingusneh2032
@hingusneh2032 Ай бұрын
does ionization of acidic compound produce negative ions ?
@deegirl6994
@deegirl6994 Ай бұрын
Thank you 🙏
@pinaldesai4559
@pinaldesai4559 Ай бұрын
Good information
@tradingworldz8629
@tradingworldz8629 Ай бұрын
2mg in 100ml 20ppm.We took 10ml volume make upto 100 ml means that's 0.2ppm.If we need 2ppm we had to take 1ml from 20ppm. Is it correct?
@gkiran3504
@gkiran3504 Ай бұрын
Sir I have questions why do we need multiple with 1000
@sabarikrish9405
@sabarikrish9405 Ай бұрын
Great work sir...❤
@AmitKumar-x5f9r
@AmitKumar-x5f9r Ай бұрын
237
@AmitKumar-x5f9r
@AmitKumar-x5f9r Ай бұрын
The most above point where all the lines are meeting