CONTENT UNIFORMITY as per I.P.
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- Опубліковано 18 жов 2024
- CONTENT UNIFORMITY as per I P.
This video will enable you to understand whole concept in very crystal clear manner about Content Uniformity and both acceptance criteria for different formulations as per Indian Pharmacopoeia.
Since we have seen that most of the person feel confused when talking about CU acceptance criteria for different formulations, so in this video specific unique game introduced, designed by presenter to understand concept of Content Uniformity in very easy, simple and user friendly language.
So be ready to Learn Simply and Earn quickly.
Thanks for explain to very easy way.
Wom amazing sir thanks for your video. It will help in interview dewe questions as b.pharama fresher
Thanks Amar, please share to your colleagues also.
@@pharmaearners7680 yes offcourse 🙏🙏🙏
Mind blowing sir
Thanks, please share to your colleagues also.
Thanks for this video’s sir👌🙏
Welcome
Thnk u so much sir for such useful information
Thanks
Thank you sir…very well explained…
Thanks Nikita, please share to your colleagues also.
One of the best vedio
Thanks, please share to your colleagues also.
Thank you sir
Thank u sir u are the best🙏
Thanks Neha, please share to your colleagues also.
Very Nice Sir Ji you are a good Teacher.
Thanks Little Angel, please share to your colleagues also
Thank you so much sir
Do it is performed in case of polyhedral tablet?
Hi Nikita, thanks for your query. can you please elaborate the dosage form.
Knowledgeable vedio sir ji
Thanks Lalit, please share to your colleagues also.
nice explanation , thanks alot sir
Thanks for appreciation. Glad you liked it. Please share to your colleagues also.
Sir your explanation is in very deep and simplest way. Please try to make videos on HPLC uv ir etc.
Thanks Rishabh, HPLC, UV videos will be published soon. Please share to your colleagues also.
Sir plz make vedio on recovery study and cleaning validation
Superb Explained
Thanks Ayush, please share to your colleagues also.
Sir please make a video on batch can be release without completion of micro results through temporary chage control
Great sir please make more and more vedios on QMS and other relevant things.
Sure, Pitaai it will be published soon.
Please share to your colleagues also.
Thanks for appreciation.
Sir content uniformity ac to bp ka bhi. Video bnao plz
Sure Kundan, same will be published soon.
Nice
Thanks Harishankar, please share to your colleagues also.
Sir cleaning validation pe video banaye
Sure, will be published soon.
Very nicely explained
Thank you so much
Very well explained 👏👍
Glad you liked it
Great sir
Thanks, please share to your colleagues also.
Sir, if test is fail then what will we do?
If conclusion comes fail, then we have to log OOS and need to do the investigation to find out the root cause.
Accordingly corrective and preventive action to be taken.
Sir mere sir bol rhe the aap glat bta rhe h 10 mg ni 25 mg api of label clam ya weight of tablet 25 percent
Hi Mahaveer, thanks for your query. 10 mg or 10% w/w IP ka criteria hai while 25mg or 25%w/w USP ka criteria hai.
Please refer the video link mentioned below;
ua-cam.com/video/mmPyGimG15o/v-deo.html
Cu accoding to bp kya hai label claim ka case
Thanks. Sir
Glad you liked it
Sir Acceptance criteria of disintegration test par video banae.
Ok
Why 85-115 range please describe
Sir! Your content is amazing ... please make a video on disintegration test apparatus
Thanks, will publish soon
Good Sir
Glad you liked it
Sir ointment cream m be uc ke vedio beno
Thanks for your query, Please listen video carefully. I hv told that for surface application formulations i. e. Crems, ointments, lotion etc. mein UOC test is not applicable.
Sir titration ka cu kaise karnge
Dear Jai Praksh, titration bhi 10 times karenge.
Dear sir please make video on content of uniformity as per usp
Sure, next video is on same topic
As per new IP 2022 updated .. can use less 25 mg CU or 25% of api
Sry sir I want you explained that in the case of 10 tables if one table assay is in between 74% to 125% …. Then the test will be pass….if not met then we have to go to the 20 tablets and the 20 tablets have must to 85-115% otherwise the test will be failed 👍
Hi Soumya, thanks for your query but in case of any content out of 10 tab at initial stage, is beyond 85 -115% but lies within range 75-125%, we must go for additional 20 units to get the conclusion for passing or failing the test parameter.
Ab update ho gya h 25 % or 25 mg ho gya
thank u so much sir
Most welcome
Thank you sir
Please share to your colleagues also
Thank you so much sir
Glad, you liked it
Thank you sir
Glad you liked it