Thank you so much sir this is very helpful for every phama students specially for me because this time I'm the member of parenteral industry i recently joined so it's much more important for me thnx again sir
Thanks for sharing... It's really nice information which you shared...I belongs to admin so it would be good for me if u share any cleaning and sanitation as well as pest control in the GMP areas
See this video What is Grade A, B, C Limits? Area classification limits and Guidelines @Pharmaven #pharmaven #iso ruclips.net/user/shortssh8FWY0HmLY?feature=share
Helpful sir, But sterile manufacturing is not perform in grade C . Although sterile manufacturing perform only in Grade A under laminor hood even aseptic manufacturing or septic.
In case API is Sterile, it is handled under Grade A. Otherwise, in case of non Sterile API, Manufacturing in Grade C, filtration in sterilized filtration vessel in closed loop, can be under Grade A, followed by filling under Grade A
Sir mere plastic product manufacturing unit hai sir mere product pharma company main supply krte hu company is asking for clean rooom envviorment classification area ap muje help kr sakte hu kaise hum iska setup kare
RLAF is to prevent spread of material, Grade should be one grade higher than surrounding area classification and may not need microbial monitoring as material handled is non sterile
Grade C aur Grade D ka particle count limit different hai. Grade C me 352000 hota hai dynamic condition me, grade D me dynamic ka koi limit nahi hai Isliye, grede C me ACPH jyada hota hai
Nice video ,In USP Monograph 797 Table 7 ( Action levels for airborne particle air sampling) shows ISO class5,7& 8 but not show ISO class 6 why? please reply .
Thank you sir for your great information....
Absolutelty great information. Really appriciated
Very good
Very informative video
Very helpful thanku sir
Thank you sir
What is Grade A, B, C, D? What is Area Clarification? हिंदी में, #aseptic #quality @PHARMAVEN #gmp
Thank you so much Sir 😊🙏
Thank you so much sir this is very helpful for every phama students specially for me because this time I'm the member of parenteral industry i recently joined so it's much more important for me thnx again sir
Well explained sir 🙏
Nice explanation sir.....keep updating
Thanks a Lot, kindly also share to your friends and groups and juniors 🎉
Very helpfull for pharma learners sir
Good one and informative
Thanks a Lot, kindly also share to your friends and groups and juniors 🎉
Thanks for Information Mr. Dhaval sir
Mujhe apki video bhut achi lagi or malomat bhi bhut hui.thanks
Thanks
Baki logo ko bhi share karna, Please
Sir ISO 14644-1 pramane pan cleanroom classifications chhe. Please explained the same by video whenever you get time. This one is amazing.
Thanks you sir for well guidance
Please also share to your friends and groups and juniors to spread knowledge 🎉
Best video ever ❤ thanks for sharing sir
Thanks🙏
Very nice sir
Thank u so much sir
After watching single video, now i m regularly watching ur videos sir..Thank u
Nice
Informative and easy explanation. We want more videos related to pharmaceutical industry
Thanks a Lot Gaurav
There are more than 250 videos on my channel, you can refer to that as well and tell me if you need something on specific topic
Great info tnx
Thanks for sharing nice information sir
Superb...
👍👍👍
Helpful sir shared & Subscribed 👍
Many Many Thanks Pramod
sir please terminal and autoclave cycle explain hindi
Very helpful sir, please share a video on regulatory affairs and API manufacturing or any channel you suggest
Sir area qualification and area classification pe vodeo baniye
Nice explanation sir.thanks
Sir Please make one video on sterile filter and air filter and there test of WIT and BPT
Sir your explanation is to good easy to learn
Can you explain HVAC validation and qualification activity
I have one video
AHU Qualification, HVAC Qualification #validation #ahu #hvac @PHARMAVEN #aseptic
ruclips.net/video/K-mpDBrqNXw/видео.html
Rodac test ke bare me btaye
Awesome sir❤
Sir question is that why class D required for tablets manufacturing
It's in Static only. Dynamic become un-classified
Sir kya tablet manufacturing mein HEPA plenum mein lga sakte?
Filling m/c principle kya hai ??
Thanks for sharing... It's really nice information which you shared...I belongs to admin so it would be good for me if u share any cleaning and sanitation as well as pest control in the GMP areas
I have one video which can help, see link below. I will prepare more based on your requirements
ruclips.net/video/wH01F9Mr3nM/видео.html
ISO aor Grade me kya difference hai...
See this video
What is Grade A, B, C Limits? Area classification limits and Guidelines @Pharmaven #pharmaven #iso
ruclips.net/user/shortssh8FWY0HmLY?feature=share
Parentral batch manufacturing kon si area me karenge b ya c a me to felling hongi
Helpful sir, But sterile manufacturing is not perform in grade C .
Although sterile manufacturing perform only in Grade A under laminor hood even aseptic manufacturing or septic.
In case API is Sterile, it is handled under Grade A.
Otherwise, in case of non Sterile API, Manufacturing in Grade C, filtration in sterilized filtration vessel in closed loop, can be under Grade A, followed by filling under Grade A
Sir mere plastic product manufacturing unit hai sir mere product pharma company main supply krte hu company is asking for clean rooom envviorment classification area ap muje help kr sakte hu kaise hum iska setup kare
Please call on WhatsApp on 9426046573
Sir why the count of nvpc is 3520 and 20 only?
Aseptic change room comes which grade
First change room can be Grade C but other should be Grade B
Area qualification karte kase hai
Sir aseptic area me dhadhi moch clean hona chhiye ya shirf daddi
Dono me se kuch bhi nahi
Clean shave chahiye
When we dispense raw material (non sterile) under RLAF, Then this area is goes to Grade A or Grade C ?
Please reply
RLAF is to prevent spread of material, Grade should be one grade higher than surrounding area classification and may not need microbial monitoring as material handled is non sterile
Grade C and D me ACPH kyu different hota he?
Grade C aur Grade D ka particle count limit different hai. Grade C me 352000 hota hai dynamic condition me, grade D me dynamic ka koi limit nahi hai
Isliye, grede C me ACPH jyada hota hai
Nice video ,In USP Monograph 797 Table 7 ( Action levels for airborne particle air sampling) shows ISO class5,7& 8 but not show ISO class 6 why? please reply .
Sir mujhe ye janna hai ki class A B C D konse pharmacopeia me milega ritten me
EU Annex 1
ISO 14644
Pharmacopeia don't have this limits
@@PHARMAVEN sir partical aur bactrial count do chahiye tha
Non parentral me kon kon se area hote hai
Is it possible grade C area LAF maintain grade A
Yes
But usual practice is to maintain LAF one grade higher than surrounding area
Cnc area me dp nahi hota hai
Sir non parentral preapration grade d me karte hai na
Sir apka name क्या h
Dhaval Surti
You can search on Google with this name
@@PHARMAVEN sir आज mera interview tha but validation k bare में jyada bta nhi paya
Kya questions ke answers nahi aye?
Bhkwas
How can I improve?
Thank you sir
What is Grade A, B, C, D? What is Area Clarification? हिंदी में, #aseptic #quality @PHARMAVEN #gmp
Thank you very much sir
Nice
Thank you sir