What is Grade A, B, C, D? What is Area Clarification? हिंदी में,
Вставка
- Опубліковано 18 лис 2024
- What is Grade A, B, C, D? What is Area Clarification? हिंदी में, #aseptic #quality @PHARMAVEN #gmp
Your Queries
1. What is Grade A
2. What is Grade B
3. What is Clean area
4. What is Aseptic area
#pharma #usfda
#cleanroom #aseptic #fda #fdaknowledge #sterile
हिन्दी में, In Hindi, Importance of Gowning in Clean Rooms @PharMaven #USFDA #pharma #aseptic
Aseptic Area Best Practices for Operators, एसेप्टिक एरिया के ऑपरेटर की ट्रैनिग कैसे करे 👍👍👍
Aseptic Area Best Practices #usfda #pharma #aseptic @Dhavalkumar Surti #gmp #sterilization #aura
please subscribe to my channel
Your Queries:-
what is aseptic Processing
vaccine manufacturing
Training
Health
How to train?
How to train aseptic Area Operators?
How to train clean area Operators!
What is aseptic Area?
What is clean area?
Basics of microbiology
Bacteria on skin
ऑपरेटर को कैसे ट्रैन करें
vaccine
FDA
warning
risk assessment
aseptic area in microbiology
aseptic technique
data integrity
data integrity pharmaceutical
depyrogenation tunnel working..
gmp
risk assessment procedures
root cause analysis examples
what is sop and how to write it
annex 1
audit para reply
Dashboa..
Content
Analytics
Comme
PHARMAVEN
aseptic area in pharmaceutical..
aseptic filling process
dhaval surti
funny lungi dance
gemba
media fill failure investigation
pharma
Sop
sop in pharma industry
audit
gmp audit
investigation report writing
How to Face USFDA Audits GMP
GMP, How to Face Audits, #pharma #Regulations #audits #success #GMP #PHARMA
Your Queries:-
How to face USFDA Audit
How to face Audit
How to be in USFDA Compliance
How to prepare for audit
Dhaval Surti
#USFDA #GMP #drug
USFDA How To Behave in Audit Room While Facing Regulatory Inspection
GMP, How To Behave in Audit Room, Facing Regulatory Inspection part 5 #audits #success #PHARMA #GMP
This video is about acceptable behaviour patterns in an audit room, talks about clothing, personal behaviour, do's and don'ts and How to help others during an audit.
How to Face USFDA Audits GMP
USFDA How to Face Audits Questions and Answers 👍👍👍👩💼👩⚖️
GMP, How to Face Audits, Questions and Answers #audits #success #Questions #answers #GMP #PHARMA
Part 2 of series About How to Face Regulatory Inspection, this part focused on How to answer questions in regulatory inspection
How to Face USFDA Audits GMP
GMP, How to Face Audits, #pharma #Regulations #audits #success #GMP #PHARMA
Your Queries:-
How to face USFDA Audit
How to face Audit
How to be in USFDA Compliance
How to prepare for audit
Dhaval Surti
How to Answer Questions in Audit
How to respond in Audit
#USFDA #GMP #AUDIT
#DHAVAL SURTI
Few Insights on How to be Successful in Regulatory Inspection in Pharmaceutical Industry, Mainly on Personnel Practices and Procedures
GMP, How to Face Audits, #pharma #Regulations #audits #success #GMP #PHARMA
Your Queries:-
How to face USFDA Audit
How to face Audit
How to be in USFDA Compliance
How to prepare for audit
How to behave in audit Room
How to dress for inspection
How to speak during Audits
Dhaval Surti
#USFDA #GMP #AUDIT
#DHAVAL SURTI
Few Insights on How to be Successful in Regulatory Inspection in Pharmaceutical Industry, Mainly on Personnel Practices and Procedures
Few Insights on How to be Successful in Regulatory Inspection in Pharmaceutical Industry, Mainly on Personnel Practices and Procedures
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
What is Grade A, B, C, D? What is Area Clarification? हिंदी में, #aseptic #quality @PHARMAVEN #gmp
Thanks for Information Mr. Dhaval sir
Thanks🙏
Thank you sir
Best video ever ❤ thanks for sharing sir
Very helpful thanku sir
Thanks you sir for well guidance
Please also share to your friends and groups and juniors to spread knowledge 🎉
Thank u so much sir
Well explained sir 🙏
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
After watching single video, now i m regularly watching ur videos sir..Thank u
Great info tnx
Very helpfull for pharma learners sir
Nice explanation sir.....keep updating
Thanks a Lot, kindly also share to your friends and groups and juniors 🎉
Good one and informative
Thanks a Lot, kindly also share to your friends and groups and juniors 🎉
Mujhe apki video bhut achi lagi or malomat bhi bhut hui.thanks
Thanks
Baki logo ko bhi share karna, Please
Thanks for sharing nice information sir
Helpful sir shared & Subscribed 👍
Many Many Thanks Pramod
Very nice sir
Superb...
👍👍👍
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
ua-cam.com/video/K-mpDBrqNXw/v-deo.html
Very helpful sir, please share a video on regulatory affairs and API manufacturing or any channel you suggest
sir please terminal and autoclave cycle explain hindi
Nice
Sir area qualification and area classification pe vodeo baniye
Rodac test ke bare me btaye
Nice explanation sir.thanks
Sir Please make one video on sterile filter and air filter and there test of WIT and BPT
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
ua-cam.com/video/wH01F9Mr3nM/v-deo.html
Sir kya tablet manufacturing mein HEPA plenum mein lga sakte?
Sir question is that why class D required for tablets manufacturing
It's in Static only. Dynamic become un-classified
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
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
ua-cam.com/users/shortssh8FWY0HmLY?feature=share
Awesome sir❤
Area qualification karte kase hai
Parentral batch manufacturing kon si area me karenge b ya c a me to felling hongi
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
Aseptic change room comes which grade
First change room can be Grade C but other should be Grade B
Non parentral me kon kon se area hote hai
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
Is it possible grade C area LAF maintain grade A
Yes
But usual practice is to maintain LAF one grade higher than surrounding area
Sir aseptic area me dhadhi moch clean hona chhiye ya shirf daddi
Dono me se kuch bhi nahi
Clean shave chahiye
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 why the count of nvpc is 3520 and 20 only?
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
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
Thank you very much sir
Nice
What is Grade A, B, C, D? What is Area Clarification? हिंदी में, #aseptic #quality @PHARMAVEN #gmp
Thank you sir