Ekdam perfect information apane Diya h Sr. AAP API production ke all equipment ke bare me information ka vedeo bana do na,jaisi ki centrifuge h, uska type,usaka size,bag kitani micron ki hoti h,etc. So plz Sr.i hope u made it.👏🙏
Sir 21 CFR doesnot have only 2 parts 210 and 211. These two parts are for Good Manufacturing practices. Ex 21 CFR part11 is describes e-signature as reliable and trustworthy as Physical signature
Vedio good because of elaborate in hindi which easy to understand.... Requested vedio to start from which guideline it is correlate.... Eg FDA , MHRA ,eurlex...
Can you describe simply by denoting giidline name and number along with 21 cfr, anvisa , ich, other guidelines. Means Which guidelines refer to validation, qualification, investigation, risk assessment, change control, deviation, incidents, capa, root cause analysis, sampling techniques, manufacturing and packing, gdp, gmp. Etc Plz awaited for response.
@@prof.karanajaygupta yeah sure, i need number and title of guidelines for above respective events and programmes. Which guidelines can refere to execute that activities
Sir FBE Air Handling Unit Pe detail video Karo,including RH,Humidifier,Dehumidifier, Dew point,Air velocity,face and by pass damper,Heating coil, Colling,filters use,drying,Explosion duct mechanism,sfm,blower,inlet damper,outlet damper,roll of each
Sir, please tell GMP GUIDELINES FOR US FDA..... ITS REALLY URGENT SIR....PLEASE REPLY???? IS CGMP GUIDELINES FOR US FDA SAME AS GMP GUIDELINES FOR US FDA????
Sir.. Ur voice tone is good.. could you please explain in English.. because I'm From Tamil Nadu.. I couldn't able to get ur videos... Or suggest me some more pages related to usfda regulatory affairs..
THANKS, NANDHINI FOR YOUR SUGGESTION . I KNOW BUT I HAVE SOME TIME LIMIT THAT'S WHY I AM CONCENTRATE IN HINDI BUT ONE DAY I WILL MADE VIDEO ON ENGLISH BUT SORRY FOR INCONVENIENCE.
Aapka diya hua knowledge bahot hume kaam aaya..apki vajah se muze job bhi lag gayi
Congratulations 👏
Thanks for this
Sir.. yor concept is very clear.. i will watch all your videos.. keep it up .. realy u r doing a great job
You are Great Prof.Karanji...
You explained the things very excellently
Thanks a lot
Thank you so much sir ... your each and every video is helping me out to upgrade my knowledge .. thank yousomuch
Nukari Jane Ki baat Sahi boli.. Knowledge puri h sir appko industry work Ki bhi
The way you explain the things....is perfect...nothing left after listening you Sir G
Excellent clarity given by u regarding 21 CFR....pls provide more to more video for pharma , so people get more knowledge...simply great
Very clear video about FDA & CFR..
21 CFR guidelines video is a very nice.
Thankyou so much.
But sir I request to you please make video on ICH guidelines and one more stability chamber.
Do what is written don’t do what you want to do
Impressive,,mera collage yaad aagge,,,this is the right way to teach.like highlighting points❤❤❤
Bahut acche tarike se explain Kiya hai sar aapane
Hello sir21cfr kya ye guidline injectable plant me used karte hai
बहुत ही अच्छे से समझाया है आपने
Bhaut achaa bataate ho bas apka video jadaa hi lengthy hai lekin apka samjnae ka tarikaa superrrrrrrrrrrrrr
Thanking you sir... I am learning u r class..
Ekdam perfect information apane Diya h Sr.
AAP API production ke all equipment ke bare me information ka vedeo bana do na,jaisi ki centrifuge h, uska type,usaka size,bag kitani micron ki hoti h,etc.
So plz Sr.i hope u made it.👏🙏
Great... Highly appritiate it...Thank you sir..Respect from Bangladesh 🙏
Really good job..I watched first time yr vedio its very good..
Thank you so much for giving precious knowledge
Too much clear information .
Thanks for this video
Crystal clear explanation
Sir plz make vedio on stability chambers
Sir 21 CFR doesnot have only 2 parts 210 and 211. These two parts are for Good Manufacturing practices.
Ex 21 CFR part11 is describes e-signature as reliable and trustworthy as Physical signature
Really good job sir, I always waiting for your new videos.
Assalam allaykum
Vedio good because of elaborate in hindi which easy to understand.... Requested vedio to start from which guideline it is correlate.... Eg FDA , MHRA ,eurlex...
Good sir 🙏 but have you any material of injectable machine like washing, filling
I love this video, truly informative....Please make a video on pharma packaging machines manufacturing, testing and documentation guidelines.
Thank you so much for sharing such good knowledge. You are a legend.... 💥
P
Wow !
Awesome video
Thanks.
Codon federal regulatory is right or not...plz correct it
Always waiting for your videos..great 👍
Sir, those slides share on side not saw properly.
Sir can you please make a video on overview of ICH guidelines.
JUST WAIT FOR MID-OCTOBER 2020.
Sir cip ka qualification kase krenge
Very informative video sir. You can be crisper in your videos and make them less long. Learned a lot of new things from you.
Sir why disinfectant filter by 0.2 micron filter
Nice learning from you sir keep going
IT ke liye bhi cfr 11 follow hota h kya?
Thank you for 21CFR Explain.
Sir ye industrial training bpharm mai sikhtey? Ye use kaha hota h?
@@jaidtechy2762
Watch #Jivyavlogs on UA-cam for Pharma /Pharmacy JOB in Dubai, Oman etc......
Sir the video is blur so I wasn't able to note down what's written on the board and also the info from the ppt...could you please help me with it
Thanx sr you are genius in pharma-knowledge
Hello sir, plz make a video on HPTLC and GC
after lockdown
Okay sir, thank you😊
21 CFR guidelines for information technology in Pharma company?
Mast samja aaj muje..thank you sir
So simple good sir 👌👌👌💯💯🙏🙏❤️
Finished product manufacturing ke bad part 211 ka kya role hai
Sir i want to 21CFR GUIDELINES
Sir aap bahut accha samjhate hai
Sir ..thank you so much..plz upload more videos regarding RA sellbus...GOD BLESS YOU SIR..
Thanks for good information..
Can you make a video on S88 Batch process
Sir Ji please tell ICH GUIDELINE
Sir very good lecture in hindi. I like it..
Sir please provide Packing department related interview questions (Blister, Bottle packing machine).for Oral solid dosage form.
You explained in a great and simple way.Thanks.
Sir, what are GMP GUIDELINES FOR US FDA..PLEASE TELL???
Very nicely described, Thanks
Any video on e ctd
Thank you sir, best explanation 😅
What is adl gide line cfr for validation
Sir you r best teacher
Sir ek question hai hplc max 2℅ rsd aur gc max 15% rsd gc me itni jayda hplc me itni kam kyu please detail me bataye
Excellent and very easy to understand
Hello sir
Wrong SOPs or unfilled or incompletely filled SOPs come under which CFR 211 subpart??
Kya 21cfr for engineering ke pdf mil sakti he
Dear sir,
Please make a video to understand commissioning in api pharmaceutical industries
Very intellectual video sir, Thanks
Sir, kindly explain how to perform validation of steam sterilizer Autoclave in pharma industry and relative best guidelines
Sir what is mean by Media fill
Hii sir
HVAC aur water system guidelines ke bare me bhi video banaye plssssssss
It's fantastic class
Plz make video on 21cfr for production area
Can you describe simply by denoting giidline name and number along with 21 cfr, anvisa , ich, other guidelines. Means
Which guidelines refer to validation, qualification, investigation, risk assessment, change control, deviation, incidents, capa, root cause analysis, sampling techniques, manufacturing and packing, gdp, gmp. Etc
Plz awaited for response.
21CFR more important as compared to the others
@@prof.karanajaygupta yeah sure, i need number and title of guidelines for above respective events and programmes. Which guidelines can refere to execute that activities
Very nice presentation pl. take on stability studies and tech transfer also.
Sir.. Serialisation p video banao na.. U tube p uski video kisne nahi Banai....
Sir FBE Air Handling Unit Pe detail video Karo,including RH,Humidifier,Dehumidifier, Dew point,Air velocity,face and by pass damper,Heating coil, Colling,filters use,drying,Explosion duct mechanism,sfm,blower,inlet damper,outlet damper,roll of each
ICH k uper b hona chye ek video
Qa la guideline kya kay hai
Very good sir.... thanks sir
Gcms ke bare Mai bataye sir
Thank you sir. Sir may I know how much industrial experience you have and in which department ?
Sir explain about 483 in pharmaceutical
thank you sir well explained 🙏🙏
Sir please one video make to the topic of Alcoa please sir
Sir, please tell GMP GUIDELINES FOR US FDA..... ITS REALLY URGENT SIR....PLEASE REPLY????
IS CGMP GUIDELINES FOR US FDA SAME AS GMP GUIDELINES FOR US FDA????
Sir, 21CFR is also folllow in API
please make video on Audit facing skill
Wow fantastic love you 💖
Sir.. Ur voice tone is good.. could you please explain in English.. because I'm From Tamil Nadu.. I couldn't able to get ur videos... Or suggest me some more pages related to usfda regulatory affairs..
THANKS, NANDHINI FOR YOUR SUGGESTION . I KNOW BUT I HAVE SOME TIME LIMIT THAT'S WHY I AM CONCENTRATE IN HINDI BUT ONE DAY I WILL MADE VIDEO ON ENGLISH BUT SORRY FOR INCONVENIENCE.
Hi Nandini, present you working which company
@@perumallachinna568 caplin steriles limited
@@nandhinis2950 were
Sir please qc qc ke subpart ki guidelines ki detail me video banaye
Great information
Very nice video sir .thanks so much
Plz make video on medical device design control
Maza aaaa gya dost
Thank for simplify this concept
Sir please tell us trs guidelines
Very nice sir please make...more detail video on deviations and investigation & CSV
Sr ich guidelines pr video btao
Sir part 11 is important for 21CFR Please explain
Very good👍
Nice explaination