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.

КОМЕНТАРІ • 80

  • @goldendanceacademy7646
    @goldendanceacademy7646 2 роки тому +1

    Thanks for explain to very easy way.

  • @AmarjeetKumar-mg6he
    @AmarjeetKumar-mg6he 2 роки тому +1

    Wom amazing sir thanks for your video. It will help in interview dewe questions as b.pharama fresher

  • @rasmirekharath2009
    @rasmirekharath2009 3 місяці тому +1

    Mind blowing sir

  • @chandrajitchandan4253
    @chandrajitchandan4253 6 місяців тому +1

    Thanks for this video’s sir👌🙏

  • @nytwalkr
    @nytwalkr 2 роки тому +1

    Thnk u so much sir for such useful information

  • @nikhitanupur1016
    @nikhitanupur1016 2 роки тому +2

    Thank you sir…very well explained…

  • @bestisyettocome2645
    @bestisyettocome2645 Рік тому +1

    One of the best vedio

  • @sanjaysarvaiya3285
    @sanjaysarvaiya3285 Рік тому +1

    Thank you sir

  • @nehapaswan1231
    @nehapaswan1231 Рік тому +1

    Thank u sir u are the best🙏

  • @littleangelcomeandplay7304
    @littleangelcomeandplay7304 Рік тому +1

    Very Nice Sir Ji you are a good Teacher.

  • @aaryagupta7655
    @aaryagupta7655 2 роки тому +1

    Thank you so much sir

  • @11nikitadhake30
    @11nikitadhake30 Рік тому +1

    Do it is performed in case of polyhedral tablet?

    • @pharmaearners7680
      @pharmaearners7680  Рік тому

      Hi Nikita, thanks for your query. can you please elaborate the dosage form.

  • @lalit5415
    @lalit5415 Рік тому +1

    Knowledgeable vedio sir ji

  • @achyutjagdhane9683
    @achyutjagdhane9683 2 роки тому +1

    nice explanation , thanks alot sir

    • @pharmaearners7680
      @pharmaearners7680  2 роки тому

      Thanks for appreciation. Glad you liked it. Please share to your colleagues also.

  • @rishabhsingh8175
    @rishabhsingh8175 2 роки тому +1

    Sir your explanation is in very deep and simplest way. Please try to make videos on HPLC uv ir etc.

    • @pharmaearners7680
      @pharmaearners7680  2 роки тому

      Thanks Rishabh, HPLC, UV videos will be published soon. Please share to your colleagues also.

    • @vibhavpandey8543
      @vibhavpandey8543 2 роки тому

      Sir plz make vedio on recovery study and cleaning validation

  • @Ayush-tk7qm
    @Ayush-tk7qm Рік тому +1

    Superb Explained

  • @deonath2ray711
    @deonath2ray711 11 місяців тому

    Sir please make a video on batch can be release without completion of micro results through temporary chage control

  • @pieudatta2965
    @pieudatta2965 2 роки тому +1

    Great sir please make more and more vedios on QMS and other relevant things.

  • @kundansah6449
    @kundansah6449 2 роки тому +1

    Sir content uniformity ac to bp ka bhi. Video bnao plz

  • @harishankarmishra7786
    @harishankarmishra7786 10 місяців тому +1

    Nice

    • @pharmaearners7680
      @pharmaearners7680  10 місяців тому

      Thanks Harishankar, please share to your colleagues also.

  • @aabhyasharma9752
    @aabhyasharma9752 2 роки тому +1

    Sir cleaning validation pe video banaye

  • @solution24x50
    @solution24x50 2 роки тому +1

    Very nicely explained

  • @zahidakhan1304
    @zahidakhan1304 2 роки тому +1

    Very well explained 👏👍

  • @funnychildren2583
    @funnychildren2583 Рік тому +1

    Great sir

  • @bhautikbhandari934
    @bhautikbhandari934 Рік тому +1

    Sir, if test is fail then what will we do?

    • @pharmaearners7680
      @pharmaearners7680  Рік тому

      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.

  • @manveersingh5894
    @manveersingh5894 Рік тому +1

    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

    • @pharmaearners7680
      @pharmaearners7680  Рік тому

      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

  • @kundansah6449
    @kundansah6449 2 роки тому

    Cu accoding to bp kya hai label claim ka case

  • @SanjayKumar-qk9px
    @SanjayKumar-qk9px 2 роки тому

    Thanks. Sir

  • @indrajeetgiree8655
    @indrajeetgiree8655 2 роки тому +1

    Sir Acceptance criteria of disintegration test par video banae.

  • @somyaamohanty5498
    @somyaamohanty5498 Рік тому

    Why 85-115 range please describe

  • @Healing_hub1
    @Healing_hub1 2 роки тому

    Sir! Your content is amazing ... please make a video on disintegration test apparatus

  • @indrajeetgiree8655
    @indrajeetgiree8655 2 роки тому +1

    Good Sir

  • @naveenkanshal2962
    @naveenkanshal2962 2 роки тому +1

    Sir ointment cream m be uc ke vedio beno

    • @pharmaearners7680
      @pharmaearners7680  2 роки тому

      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.

  • @jayprakashkanaujiya2397
    @jayprakashkanaujiya2397 2 роки тому +1

    Sir titration ka cu kaise karnge

  • @praveengupta4047
    @praveengupta4047 2 роки тому

    Dear sir please make video on content of uniformity as per usp

  • @maheshgupta564
    @maheshgupta564 Рік тому

    As per new IP 2022 updated .. can use less 25 mg CU or 25% of api

  • @soumyaswain1490
    @soumyaswain1490 2 роки тому +1

    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 👍

    • @pharmaearners7680
      @pharmaearners7680  2 роки тому +1

      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.

  • @akshaypundir2707
    @akshaypundir2707 Рік тому

    Ab update ho gya h 25 % or 25 mg ho gya

  • @zaibunnisa2836
    @zaibunnisa2836 Рік тому +1

    thank u so much sir

  • @drxbittuchauhan5712
    @drxbittuchauhan5712 2 роки тому +1

    Thank you sir

  • @goldendanceacademy7646
    @goldendanceacademy7646 2 роки тому

    Thank you so much sir

  • @Aap.927
    @Aap.927 2 роки тому

    Thank you sir