CLEANING VALIDATION PHARMACEUTICAL INDUSTRY IN HINDI, cleaning validations basics
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- Опубликовано: 12 сен 2024
- This video deals about the cleaning validation concept in pharma industry. How do we perform cleaning validation and what are the methodology we use to do the same .
Very nice satyam Babu ..
Wow, good explanation for freshers.
Good 👍
Really nice content with best explaination
Wonderful presentation
Thanks a lot
Nice video sir. Idea clear ho rahe hai. Kuki meri English Itani achi nahi hai to English padh kar samjna bahud muskil tha, apne easy kar diya. Thank you. apka video ke end me ek do example idea acha hai pura idea udhar hi clear ho jata hai. Har ek video ke bad examples diya kijiye. Thanks
Thanks dear to like my video, meri bhi yahi koshish hia ki mai aap jaise baki logo ko help kar saku guidlines ka matlab samajhne me. Agar mera video achcha laga to ise age share kijiye taki or b logo ko isse Fayda ho sake, or han mere channel ko subscribe zaroor kijiyega. Thanks
Sir liquid oral department me kaise cleaning validation hota hai us bare details chaiye.
Nice job 👍
Nice explained sir.kindly upload API production related all video.
Arrey kaha chale gaye sir bht miss kr rhe the.. Very nice...
Are yahi hu tum logo k pas kaha jaunga
Thanku so much sir 🙏
Hello,
Very informative video.
Can you explain how to calculate MAXCONC limit with an example?
Hello Nishit, definitely I will explain but these days I am in some personal trouble and probably 1.5- 2 months wouldn't be able to post any thing, so sorry for that, after 2 months surely will explain all your queries
Sure y not but can't update in existing video, will surely try to make a separate video on said query
Very nice
Thank you sir plz make more videos
Sure I will
Very nice 🙏
Really it’s very knowledgeable video.
I loved the way u explained it
Thanks a lot dear
I just want to suggest you to check the SF mentioned for sterile preparation
Sorry dear, I didnt get your point
Safety factor for topical is 100, for oral is 1000 and for sterile is 10000 but you mentioned as 10
OMG that was a typo, thanks to mark d same, but unfortunately now I can't correct the same. But any way Iwill take care in future. Thanks a lot to let me know
@@dattatrayunde7089Right
Nice
Thanks
Tq sir
Dear sir, your last video was 9 months ago. Why don't you upload your next videoes? Your videoes are really excellent. This is first my comment for any RUclips channel beacuse we need your videos.
well mr. bakir thanks a lot for your valuable comment, even you are the first person who pointed out dat u didn't make a video so long. Well as i am i volved in some of my other projects dts y not getting ti.e to make videos but very soon i will make some more jntresting and informative videos for mt subscribers.
Nice video liked it. Also explain cleaning solvents selection or insoluble drug cases if you can update this video.
Thanks to like d video, and I will try to update the same in next video.
Dear I can't update existing video but will make a separate video on said topic
thanks for this excellent vedio lecture
Thanks dear for liking the video
Please make video on system validation.
sure dear
Nice information sir
Thanks dear
Make a video on area qaualification
Very nice and help full videos
Thanks sir
Thanks dear
Thanks sir
Welcome
Sir you are requested to make videos on retain sample management and stratified sampling
Ok dear
Thank u sir keep it up and help us
Always welcome
Sir, very informative
Thanks a lot dear
You explained very nice.. Thank you sir
Thanks dear
Sir line clearance par ek video banao plz
Sure dear
Any rang of NOEL...MACO....PPm criteria....that is good or bad patient
Sorry dear didn't get your query.
Nice video sir..
Can u plz tell me about the solvent used for swab stick & how to calculate the recovery study of cleaning agent..
Well dear generally we use water as a solvent agent for cleaning validation.because we need to wash our equipment with water only. In case some specific material is there which is hard to clean dn we will use agent accordingly. Recovery study of cleaning agent is generally by verifying conductivity. Detail I can't explain with massages only.
Thanks for d reply sir.. 🙏
My qst. is, In case the product is "practically insoluble in water" then i thought it doesnt come in swab. So it is under LOD & cant detected in analysis.
For recovery study i request u to plz make separate video. It is vry helpful for us...Thanks
@@vikramsinghrathore6826 yes exactly that's y I said if any substance is not soluble then we will go for the mother solvent in which it may dissolve
It's really good sir if possible please send me the example of material we chose with protocol and report for better understanding
Mail id.vijayinorg@gmailcom
Mob.9110409993
Thanks Dear for liking the video. Well right now it is not possible to send you such material but in future I will definitely start some program to provide material also. Except this what ever query you have you may ask.
👍👍👍🙏🙏🙏🙏
Thank you so much sir
Most welcome
sir can you make a video regarding wfi
well dear what u know abt wfi
sir how can I consider the previous product or the next product in MACo calculation please reply 🙏
Sir bta do please previous product or next product kese pta chlega. Agr solubility km hai or Ld 50 km h or therapeutic daily dose km usko previous product consider krenge kya. Or phr next product kisko consider krenge please reply sir 🙏
sorry dear mai aapka question theek theek nahi samjh paya
Sir please make a vidio regaeding Equipment qualification
Dear go to my channel you will get video for qualification also, or if you will ask I will share the link
Sir, I request you to also have a video on qualification
Sure I will
Qualification is video bana diya dear dekh lo
Dear Sir
Please explain what is the difference between Deviation and Event in pharmaceutical industry and give examples. I am confused literally between which one is deviation and which one is event. If one person did not wear his gowning in production is this event or deviation? One manufacturing step not followed is this event or deviation ?
dear you may read my reply for same question in my deaviation video
Very nice sir 👍👍
So nice of you
Very nice sir.. Can u explain sir that how to decide ppm solution for lod loq test in cleaning validation and method validation?
Definitely dear but these days I am quite busy with one of my very important project, so you will definitely get your answer but after few days. Thanks to like the videos, please share the same with your known also.
Sir kindly guidline reference bhi btay
Ok dear I will take e care
@@loveforpharma934 thanks for possitive response
@@loveforpharma934 love from pakistan and Happy independence day
method velidation kya hai?
To validate the prescribed method of analysis wether in pharmacopoeia or it could be in house
i want to know about class A B C and CNC, and balanceing of clean room. pl help
Well dear for this I need to make a proper video dn only I can cover all said topics. Hopefully will make said video soon.
which recherche pepar you have tack sir?
none
Sir is lockdown me kuch naya vidio bnaao
Gmp vs cgmp
Ok sure dear
🙏👍👍👍
Sir why you have used word detergent?
beacuse some of the plants are still using detergents
Minner cleaning is b type cleaning
no A type
Sir blister or strip packing machine pa koi vedio banio na plx
Well dear definitely I will make videos on said topics but due to lock down I am stocked some where to till lockdown I am unable to make my video, so please wait till lock down for my next video.
Good informative, can you pls explain about swab limit calculation
Well y not but for that I need to to make another video for this particular topic, probably will cover in future. Thanks for watching and to like the video, plz share the video with your known once.
2 month ho gaye sir ab to GMP vs cgmp pr video bna do plzzzz
Ofcourse dear on your demand only I made video on cleaning validation first, right now I am busy with some important assignment but very soon you will definitely get your video
Sir iska pdf link bejan
Dear it's a video
@@loveforpharma934 ppt sir
@@hardeepjangra533 sorry dear we dont provide study materials yet, may b in future I shall provide