PROCESS VALIDATION I PART-1 I INTRO I IMPORTANCE I HINDI

Address for person and students who are interested in training and consultancy service-
B.R. NAHATA COLLEGE OF PHARMACY, NEAR KRISHI UPAJ MANDI, MHOW- NEEMUCH ROAD,
MANDSAUR (M.P.) 458001
PHONE NUMBER-9501846476, 9630301810
E MAIL ID-(1) [e-mail] (2) [e-mail]
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Disclaimer - video is for educational purposes only. Copyright Disclaimer Under Section 107 of the Copyright Act 1976, allowance is made for "fair use" for purposes such as criticism, comment, news reporting, teaching, scholarship, and research. Fair use is a use permitted by copyright statute that might otherwise be infringing. Non-profit, educational, or personal use tips the balance in favor of fair use.
THANKS FOR WATCHING.
#VALIDATION #PROCESS #QA #QC #PHARMA #INDUSTRY #NAUKRI #JOB #INTERVIEW

[@coolstudio120]

I like your teaching style

[@syedmbilal7741]

One of my most awaited topic by karan sir😉😊

[@stockspower3410]

Jabardast

[@hemantbramhne4435]

one correction . Process validation is a continuous process. Concurrent validation is life long process undertaken in different time phases. e,g, new product, first 30 batches data collected at each and every stage is thoroughly scrutinized. after this QA will suggest different time line,e.g.every 15the batch for 6 months, every 50th batch for 1 yr etc. Any repairs undertaken may also need re validation ( same by same Vs same by different) , off course not of the whole process. Actually posting of new person ( promotions, change of job etc)for handling of critical process also may need re validation. 3 M ( Man,Material and Machinery) issue.( All these details will take around 10 lectures)

[@yogitamane4246]

To much easy ...... thank you

[@Rahul34129]

Thank you sir

[@AbhijeetAjanikar]

Can you please make video on system suitability parameters and calculation... thank you

[@walimuhammadpanhwar453]

Well explained

[@captainpharma1315]

sir i watched your every video and everytime i learnt in brief i think u shld open a training centre in baddi too as it is pharma hub.I want to learn QC instruments but there is no training centre.

[@VijaynathShukla]

Good explanation sir for process validation

[@dayalsingh7592]

Nice sir..

[@zahraaouaidjia9808]

Please try to do your courses in English to reach larger audience (at least provide English subtitles). I am Algerian, very interested in the subject but unfortunately I don't understand you.

[@dattatrayadighe6907]

Bahut achha explain karte hai sir

[@Drx.deeptigautam]

thanku sir 🙏

[@poolguy266]

Wow , mujhe sab samaj raha hai

[@rahulkulkarni2738]

Plz suggest which guidance use for process validation

[@vaishnavidahalkar7969]

Thanks sir ji 🎉

[@umabhatnagar8343]

👍

[@shan_kar0303]

Guru g kya aap materials se related series bna skte ho ? Complete characteristics of API and Excipients..5-10 in each video.

[@aabhyasharma9752]

After send sample marketing. Stability study ,continous shelf life plus one year.

[@hemantbramhne4435]

Yes, under the advised storage conditioons (validated)

[@hemantbramhne4435]

Forgot one more thing. Small batches produced in /by QC, have to have a logic. e.g. parameters defined after making batch of 1000 tabs/product can not be extrapolated to make a batch of 100000. In this example it is good idea to make batch of 15000-25000.

[@bhaskarlakavath]

Sir can you update GC calibration

[@sushilkumarpal4612]

Sir sample size kaise decided karte hai kitna gram kis stage se lena hai

[@sachinsharmavadodara]

Nice

[@priyankashinde8897]

Nice explanation

[@bhavnarajguru3689]

Please make a video for vendor questions and related certificate/declarations like a TSE BSE ,GMO etc and importance of this declarations

[@AkhtarAli-vv6nk]

How one can validate process for determining the a sodium benzoates in ketchup by spectrophotometer

[@rohitkumar-wk7sc]

Sir double door autoclave , calibration and validation ka video bano ... Aap

[@mohammedasif7667]

Make some videos on MEDICAL DEVICES INDUSTRY PLSSSS

[@yaginichandrakar6659]

Very nice

[@myworld4525]

Also known as preformulation

[@manushyamitra2583]

Thnx sir❤

[@prof.karanajaygupta]

🙏🙏🙏🙏

[@vaibhavshinde10]

Sir aap acha explain karte ho But jyada lenghthy ho jata hai

[@NeetuDx99]

Sir Exhibit Bach k bari Ak video bana do pzz

[@vishalyadav-cg5og]

Good morning sir.. I am vishal Yadav from lucknow pursuing b. Pharm 3rd year 5th semester.............. Sir mujhe industry training karna hai........... But mujhe koi ideas nhi h kaise aur kaha se karuu........ Aap kuch help kar sakte hai???

[@AdilKhan-ek7sz]

Liquid department me process validation kaise karte hai is bare me details chaiye

[@hemantbramhne4435]

1 fandamental bat yad rakhiye. Har wo chiz/bat/action jisase product reliability pe farak pad sakata wo bilkul documented correct honi chahiye.Har product ki jaroorate alag hoti hai, Basic samaz gaye to khud hi design kar sakenge.e.g. koi bhi liquid agar final product me jane wala hai to uske liye ss316L containers/pipeline hi use honge 306 nahi chalega.

[@girasegopal5323]

Sir agar process validation mai document main wrong entry ho jaye to kya hoga?

[@hemantbramhne4435]

Pahale ye proove karana padega ke sirf" entry galat hai"( human error). (e.g. 1.1 ki jagah 1.01 likha gaya)Isiliye sara raw data, calculations= sheets rakhani padati hai.Sara raw data study karake QA data correction karega. data correction me whitener ect nahi chalega purana data strikethrough karake nayi entry countersignature ke sath QA approve karega.

[@girasegopal5323]

Aur sir agar A.R no Generat nahi kiya he means TR recieved nahi hua he aur analysis ho gaya he aur TR par sign/date bhi laga diya he to kya kare?

[@ydb6061]

Sir HPLC ka validation ka video hai kya ??

[@hovsac3467]

Why u repeat one sentence 4 to 5 times..😅😅

[@kpentertainment5650]

Are sir jo topic he wahi sikha de na re baba tu...exam ke pehle hi dekhte video students aapko kya lagta hai free time mai yahi dekhte hai kya....pura history mai jate hai koi jururat bhi nai