Video není dostupné.
Omlouváme se.

Cleaning Validation

Sdílet
Vložit
  • čas přidán 16. 08. 2024
  • This training video will insight on Cleaning Validation - Inspection observations, Visual clean criteria & Solving practical problems during cleaning validation.
    Pharmaguideline, NSF International,LEARNINGPHARMACY.IN
    Cadila, Sanofi,Zydus, AstraZeneca,Mylan,Interview Questions with Sharma Ji,ASK Mechnology,emainfo,Qualistery - GMP Content,easy medical device

Komentáře • 58

  • @hitendrakumarshah3718
    @hitendrakumarshah3718  Před 5 lety +3

    This training video will insight on Cleaning Validation - Inspection observations, Visual clean criteria & Solving practical problems during cleaning validation.

  • @shahrzadtalebian8086
    @shahrzadtalebian8086 Před 4 lety +1

    very informative. I subscribed to your channel and watched most of your videos. Subtitle is always useful. Thanks for adding it. Now I can follow and understand your explanations.

    • @hitendrakumarshah3718
      @hitendrakumarshah3718  Před 4 lety

      Thanks and welcome. Keep Learning !!! The video will be available soon on,"Inspection Readiness for computerised systems". You will get notification shortly about it if, you have activated notification icon(BELL) button.

  • @aneeshkumarpatel2811
    @aneeshkumarpatel2811 Před 4 lety +1

    A lot of thanks, very helpful.

  • @JC-qu1se
    @JC-qu1se Před 4 lety +2

    Sir i have a query for one cleaning validation.
    If my product concentration is 50 MCG per ml
    And batch size is 275 litre.
    What should is acceptance criteria.

    • @hitendrakumarshah3718
      @hitendrakumarshah3718  Před 4 lety

      We can not just evaluate by referring this information. I suggest, you refer our cleaning validation part- II for better understanding. I am sharing link for the same. czcams.com/video/zBLqRZ5DXV4/video.html

  • @user-ww4vq5ld7b
    @user-ww4vq5ld7b Před 10 měsíci +1

    Voice re sound is coming in most of the videos ,if it rectify more advantage to audience

  • @venkatakrishnaanil
    @venkatakrishnaanil Před 4 lety +1

    Good presentation

  • @yashshah8706
    @yashshah8706 Před 4 lety +1

    Very nice and helpful.

  • @mahendrasinhchavda3948
    @mahendrasinhchavda3948 Před 2 lety +1

    Sir very useful video for me 👌

  • @ashishjain412
    @ashishjain412 Před 4 lety +1

    Nice video

  • @myfriends446
    @myfriends446 Před 5 lety +1

    Good explanation Sir...

  • @manoharkallapari8765
    @manoharkallapari8765 Před 2 lety +1

    Sir plz do videos about cleanability study,DEHT and CEHT

  • @MrKrish1029
    @MrKrish1029 Před 3 lety

    Is this cleaning validation shall be done with respect to every product on every equipment?? suppose in a non dedicated commercial manufacturing plant product A manufactured 10 batches on a row and for first three bathes company has performed cleaning validation, established dirty equipment hold time and cleaned equipment hold time as well, after product change over product B is going to manufacture in same equipment train which are used earlier for product A, now product A cleaning procedure, dirty hold time and cleaned equipment hold time is applicable for product B or not, please clarify.

    • @hitendrakumarshah3718
      @hitendrakumarshah3718  Před 3 lety

      I suggest you to go through below two recorded webinars to get more understanding
      czcams.com/play/PLq7ln35Rt1rMN52n2o3t_nH0lpmZShkZ6.html

  • @venugopalsriram
    @venugopalsriram Před rokem +1

    Can you please provide the qualification procedure of person for visual cleaning

    • @hitendrakumarshah3718
      @hitendrakumarshah3718  Před rokem

      You can qualify the person/operator after cleaning and testing the swab or rinse residue.

  • @cosmeticgmp
    @cosmeticgmp Před 4 lety +1

    good work, thanks!

    • @hitendrakumarshah3718
      @hitendrakumarshah3718  Před 4 lety

      Thank you so much for your kind appreciation. If you need any support, please feel free to contact me.

  • @shobhalatha5048
    @shobhalatha5048 Před 4 lety +1

    Informative and helpful for professionals
    Post DI Issues Videos

    • @hitendrakumarshah3718
      @hitendrakumarshah3718  Před 4 lety +1

      Sure. The upcoming video will be DI issues and audit trail compliance. Thanks for your suggestion

    • @hitendrakumarshah3718
      @hitendrakumarshah3718  Před 4 lety

      Hope, you watched the DI video.
      czcams.com/video/YUszNGe6Uyk/video.html

  • @PankajSharma-ym4je
    @PankajSharma-ym4je Před 3 lety +1

    Helpful video sir, please provide information about CV for TF

  • @PankajSharma-ym4je
    @PankajSharma-ym4je Před 3 lety +1

    Sir TF means Topical formulation, how calculate MACO for all criterias for TF

    • @hitendrakumarshah3718
      @hitendrakumarshah3718  Před 3 lety

      I suggest, you can go through complete cleaning validation package. You will get information on all sort of dosage forms.If you have any questions, please feel free to comment. Will revert you. You can access the cleaning validation package through the link below;
      czcams.com/video/zA5xsWR9IU8/video.html

  • @shivkumarbeenaboina5853
    @shivkumarbeenaboina5853 Před 3 lety +1

    Dear sir please make a brief video on environmental monitoring program in formulation (injectable).

  • @MohsinKhan-ix9ws
    @MohsinKhan-ix9ws Před 5 lety +2

    Respected sir plz make video on audit trail and it's compliance and how to check audit trail

  • @abhijeetgaikwad4202
    @abhijeetgaikwad4202 Před 4 lety +1

    Will you provide IPQA whole resposibilities

    • @hitendrakumarshah3718
      @hitendrakumarshah3718  Před 4 lety

      The responsibilities are inprocess at shop floor, evaluate critical process parameters, evaluate cleaning activities and give line clearance before going ahead for new product so as to protect the next product from contamination. Now a days, IPQA role is considered as Quality facilitator.

  • @akashrathore8630
    @akashrathore8630 Před 4 lety +1

    Needed good editing

  • @DineshYadav-ni2cm
    @DineshYadav-ni2cm Před 3 lety +1

    For general cleaning watch below presentation, then after CV,
    czcams.com/video/xv8rwmKe0Ok/video.html

  • @shailendra1277
    @shailendra1277 Před 4 lety +1

    Excellent Hitendra.

  • @gauravsharmamtvnlvideos
    @gauravsharmamtvnlvideos Před 4 lety +1

    Sir, please give the training about how to do cleaning validation as per fda guidelines

    • @hitendrakumarshah3718
      @hitendrakumarshah3718  Před 4 lety +1

      Dear Gaurav, I will really like to take training on this topic, if approximate 10-15 participants are available. Request you to check with your subordinates and friends. Please confirm.

    • @ashishjain412
      @ashishjain412 Před 4 lety +2

      @@hitendrakumarshah3718 I am interested for cleaning validation topic

    • @hitendrakumarshah3718
      @hitendrakumarshah3718  Před 4 lety

      @@ashishjain412 Sure. We will take up this topic as well.

    • @hitendrakumarshah3718
      @hitendrakumarshah3718  Před 4 lety

      @@ashishjain412 We will plan next week for online training(webinar) on cleaning validation.

  • @Vishalchaurasiabpharm
    @Vishalchaurasiabpharm Před 4 lety +1

    How to perform for vaccine

    • @hitendrakumarshah3718
      @hitendrakumarshah3718  Před 4 lety

      For cleaning validation after vaccine product, we need to evaluate what factors will impact on next products e.g. antigens of previos virus vaccines, the chemicals used for attenuation etc. We need to evaluate traces of these antigens or chemicals. It all depends on process followed. If you specify in detail, can guide you in better way.

  • @shirishareddyvlogskurnool6605

    Voice was dnt good ....pls request before taking vidoe pls make ensure and do it all

    • @hitendrakumarshah3718
      @hitendrakumarshah3718  Před 4 lety

      You are right. In this video, I have not used collar mike hence resulted in to some echo. After this video, I started using collar mike.

  • @yogeshkhule5456
    @yogeshkhule5456 Před 4 lety +1

    Nice video