QUALITY RISK MANAGEMENT IN PHARMA, QRM IN PHARMA, FMEA, HACCP, QUALITY RISK ASSESSMENT.

Поділитися
Вставка
  • Опубліковано 2 жов 2024
  • This video is all about the QRM I.e. Quality Risk Managenent in pharma. The tools, the methodology used to manage the same is explained in this video.

КОМЕНТАРІ • 98

  • @bharti3080
    @bharti3080 9 місяців тому +2

    Kl paper h mera or aaj itne month baad sahi content mila or itna easy explanation 😂 mujhe av yaad bhi ho gya +smj bhi gyi av paper m y question toh nhi chutega

  • @deepakshukla7782
    @deepakshukla7782 2 роки тому +5

    Please explain with some examples and give some tick how to identify max.causes,effect,and occurence in best possibility way

    • @loveforpharma934
      @loveforpharma934  7 місяців тому

      Well dear please elaborate ur question I didn't get what u want to ask

  • @prafultiwari6471
    @prafultiwari6471 Рік тому +1

    sir slides ko full screen ka rakha karo taaki clearly dikh sake

  • @prasannabattula6500
    @prasannabattula6500 Рік тому +1

    Sir please explain other tools also

  • @sandeepsinghkaler290
    @sandeepsinghkaler290 3 роки тому

    Sir very nice video and please upload a video on validation protocol and report of product with draft copy and please suggest what are variables we have consider while manufacturing of tablet

  • @shivalikakhandelwal5051
    @shivalikakhandelwal5051 Рік тому +1

    Hi sir
    Do you have an explanation on process validation
    Can you provide a link pls

  • @shaikhshahedahemad5299
    @shaikhshahedahemad5299 3 роки тому

    Ap ki aawaz saaf nahi ati hai

  • @sachinpandit7786
    @sachinpandit7786 3 роки тому +1

    Hello sir I am regular review your vedio .I want to ask why is requirement of risk assessment and impact assessment.why need to this

    • @loveforpharma934
      @loveforpharma934  3 роки тому

      thanks dear, for waching. As i told my risk assessments were perorm to detect, evaluate and eliminate the quality issues within the manufacturing process.

  • @bharti3080
    @bharti3080 9 місяців тому +1

    Kl paper h mera or aaj itne month baad sahi content mila or itna easy explanation 😂 mujhe av yaad bhi ho gya +smj bhi gyi av paper m y question toh nhi chutega

    • @loveforpharma934
      @loveforpharma934  7 місяців тому

      Thanks dear good to hear that my explanation can help you for your paper, best of luck for your papers, also share my videos to your friends so can they also get these explanations in easy way

  • @Robinsingh-lf9cj
    @Robinsingh-lf9cj 3 роки тому +1

    Thanks you sir document ke sath equipments ke bare me eshi tarah video bnayiye exp.About .SSR. GRL .CENTRIFUGE .FBD
    EXTRA I am waiting your video

  • @tankkapil9867
    @tankkapil9867 3 роки тому +1

    Cfr 21 ka video banaiye

  • @ajaymeena4509
    @ajaymeena4509 3 роки тому +1

    Thanks sir again video upload 👍

  • @neetaabhale9385
    @neetaabhale9385 3 роки тому +3

    Thank you sir! very well explained

  • @hemantsuryawanshi422
    @hemantsuryawanshi422 3 роки тому +1

    U r doing excellent work sir.
    Thanks

  • @mansouralajeemi9101
    @mansouralajeemi9101 2 роки тому +1

    hello doctor
    first thanx for video and second as we are student from abroad speak english
    can we ask to provide those videos in english?

    • @loveforpharma934
      @loveforpharma934  Рік тому

      Thanks dear, actually dear I prepare these videos for those candidates who were week in English. There are lot of videos for these topics in English on air but very few were there to teach in English. But dont worry I will make videos in English also.

  • @chaudharyabhinavsinsinwar5374
    @chaudharyabhinavsinsinwar5374 2 роки тому +1

    thank u sir for this brilliant explanation

  • @divyadixit6307
    @divyadixit6307 3 роки тому +1

    General statistical approaches for retest period par koi video hai kya aapki

  • @samvdio7513
    @samvdio7513 3 роки тому +1

    Nice but explain with pharma example onl

    • @loveforpharma934
      @loveforpharma934  3 роки тому

      Well dear I choose those examples with whom we can correlate easly that's y I only choose use to examples.

  • @shanyarajput1169
    @shanyarajput1169 2 роки тому +1

    Nicely explain

  • @eramshaikh_21397
    @eramshaikh_21397 2 роки тому +1

    very very helpful sir

  • @Aa-007
    @Aa-007 Рік тому +1

    Sir please provide slide of QRM ..

    • @loveforpharma934
      @loveforpharma934  7 місяців тому

      Well dear you can take screen shot from d videos

  • @ajaymeena4509
    @ajaymeena4509 3 роки тому

    Next topic video upload

  • @ajaymeena4509
    @ajaymeena4509 3 роки тому +1

    Very good sir

  • @ganatheneha6363
    @ganatheneha6363 3 роки тому +1

    Thnx for thiz video
    Helped a lot 👍

  • @nileshkushwah4488
    @nileshkushwah4488 3 роки тому +1

    Ultimate sir nice video ....thanks for this.

  • @AarvikaMulgir
    @AarvikaMulgir 2 роки тому +1

    Sir please share notes

  • @gauravsaini2080
    @gauravsaini2080 3 роки тому +1

    Nice information
    Thank you.

  • @simranmandhan3115
    @simranmandhan3115 2 роки тому

    Kappa?? Meaning??

    • @loveforpharma934
      @loveforpharma934  2 роки тому +1

      its not kappa CAPA i.e. Corrective Action and Preventive Action.

  • @waradenitin128
    @waradenitin128 3 роки тому +1

    Hello Sir, Please Share one Video for Types of Sampling in Pharmaceutical Industry

  • @AnilKumar-iy7hf
    @AnilKumar-iy7hf 2 роки тому

    Sir Good explanation....pl. explain the RPN Caleculation by using Severity probability detectability...tq..

  • @omprakashkumar6355
    @omprakashkumar6355 Рік тому +1

  • @vilaspawar6605
    @vilaspawar6605 3 роки тому +1

    Thank you sir for teaching easiest way

  • @SumanSharma-jl1bk
    @SumanSharma-jl1bk Рік тому +1

    👌👌👌

  • @udaypratapthakur5395
    @udaypratapthakur5395 3 роки тому +1

    Sir , please explain risk assessment

    • @loveforpharma934
      @loveforpharma934  3 роки тому

      Dear QRM hi risk assessment hai or ye video usi k bare me hai

  • @simranmandhan3115
    @simranmandhan3115 2 роки тому +1

    Wowowo

  • @sachinpandit7786
    @sachinpandit7786 3 роки тому +1

    Very nice vedio

  • @jrpmarket8538
    @jrpmarket8538 3 роки тому

    great explanation sir g !! thanx

  • @IrfanKhan-sn9pd
    @IrfanKhan-sn9pd 3 роки тому +1

    attractive manner

  • @jivi7343bijnoramrohau.p.
    @jivi7343bijnoramrohau.p. 2 роки тому

    Excellent work sir

  • @vikaspachisia5090
    @vikaspachisia5090 2 роки тому

    Awesome 👍

  • @pharmaindustry1912
    @pharmaindustry1912 3 роки тому +1

    Good job

  • @Mr0000DJ0000
    @Mr0000DJ0000 3 роки тому

    Sir AQL Explain it

  • @kundansinghsuner4107
    @kundansinghsuner4107 3 роки тому

    Thank you sir
    Please make a vedio on calibration of weighing balance

  • @amrutasworld8751
    @amrutasworld8751 3 роки тому

    Excellent

  • @pharmasolutionpakistan7668
    @pharmasolutionpakistan7668 3 роки тому +2

    Sir very good struggle I appreciate u being a teacher

  • @advancegamer88
    @advancegamer88 3 роки тому

    sir it is pre or post management tool?

  • @santoshkawade8751
    @santoshkawade8751 2 роки тому

    Very nice information sir

  • @rakeshkumarsingh2573
    @rakeshkumarsingh2573 3 роки тому +1

    Sir with out line clearance production ne manufacturing me batch start Kar diya to kya risk management karenge

    • @loveforpharma934
      @loveforpharma934  3 роки тому

      bilkul ye to pahle hi risk assessments me cover ho jana chahiye,for now iske ljye incident n NCR file karenge.

  • @siddharthzala2652
    @siddharthzala2652 3 роки тому

    🙏🙏🙏🙏🙏

  • @shwetathakur3158
    @shwetathakur3158 3 роки тому

    Sir what is the difference between impact assessment and risk assessment ?

    • @loveforpharma934
      @loveforpharma934  3 роки тому +1

      Impact assessment we perform after implementation or after held any any process, while risk assessment is perform before implementation of any process

    • @shwetathakur3158
      @shwetathakur3158 3 роки тому +1

      @@loveforpharma934 Thnku sir bt samajh nhi aaya . Can u explain in detail with example

    • @loveforpharma934
      @loveforpharma934  3 роки тому +1

      @@shwetathakur3158 well dear when we go for an routine practice like we need to go for material receiving dn we do risk assessment,but when we do go for any change in routine practice dn we do impact assessment like in same material receiving we now eliminate g any routine practice like weighing of material dn what it will make an impact dt we have to analyze

    • @shwetathakur3158
      @shwetathakur3158 3 роки тому

      @@loveforpharma934 ok sir thnku

  • @ETHAN_HANT
    @ETHAN_HANT 3 роки тому +1

    Sir your information is very useful can u explain quality control and quality assurance role in pharmaceutical industry