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- เผยแพร่เมื่อ 19 ม.ค. 2024
- What is Grade A, B, C, D? What is Area Clarification? हिंदी में, #aseptic #quality @PHARMAVEN #gmp
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1. What is Grade A
2. What is Grade B
3. What is Clean area
4. What is Aseptic area
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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
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How to train clean area Operators!
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ऑपरेटर को कैसे ट्रैन करें
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How to Face USFDA Audits GMP
GMP, How to Face Audits, #pharma #Regulations #audits #success #GMP #PHARMA
Your Queries:-
How to face USFDA Audit
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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
Good information sir
Sir please make video on cleaning validation
👍👍
Engineering ke liye bhi vedio banaye.
Thank you sir..
Thank you sir
Thank you Sir!
Sir, please make video on new stability chamber qualification.
Sir passbox LAF cabinet ko rest or operation me kis grade me NVPC krna chahiye
It should be equal to cleaner grade of area where it opens
What if take the measurements in cubic feet ? Will the sampling time be reduced?
Very useful video sir , I have a question I understood about the critical points as you had described it already in this video, so sir what would be the non critical sampling location/points? Thanks
Non critical locations are those where there are no open sterile containers, no interventions, no fillings or stoppering is done,
For example, after vial is sealed, there is no exposure of product to open atmosphere hence that section is not critical
In area, where there is no man material movement, material storage , for example, corners of room, locations near filling machine where there is no intervention or operator activity are non critical locations
We don’t have to do any monitoring on non critical locations
Great , thanks so much sir for the reply.. it was very helpful
I have also prepared video for that
Table A.1 is applicable for non-viable locations or both viable & non-viable both ?
Only non viable
Can we use DI water in autoclave for steam generation
Does your autoclave is with in built steam generation?