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PHARMAVEN
Индия
Добавлен 11 авг 2012
Pharma Knowledge Sharing Channel
#usfda #pharma #injectables #aseptic #bacteria #sterile #sterilization #Dhavalkumar
Dhavalkumar Surti, RUclips Channel titled 'PharMaven' for sharing knowledge about Pharmaceutical Industry
GMP Trainer, Pharma Professional, Regulatory Compliance, USFDA Exposure, Motivational Speaker, Life and Philosophy Experience Sharing, Thinker, @dhavalkumar Surti, #USFDA, #GMP, #pharma @Dhavalkumar Surti, #aseptic, #media fill, #how to face audits, #sterilization, #smoke study, #autoclave, #freeze, #drying, #smoke, #incident, #investigation, #gemba, #walk, #SOP, #humanerror, #CAPA, #breakdown #trending
#usfda #pharma #injectables #aseptic #bacteria #sterile #sterilization #Dhavalkumar
Dhavalkumar Surti, RUclips Channel titled 'PharMaven' for sharing knowledge about Pharmaceutical Industry
GMP Trainer, Pharma Professional, Regulatory Compliance, USFDA Exposure, Motivational Speaker, Life and Philosophy Experience Sharing, Thinker, @dhavalkumar Surti, #USFDA, #GMP, #pharma @Dhavalkumar Surti, #aseptic, #media fill, #how to face audits, #sterilization, #smoke study, #autoclave, #freeze, #drying, #smoke, #incident, #investigation, #gemba, #walk, #SOP, #humanerror, #CAPA, #breakdown #trending
CIP Cycle Spray Ball Coverage and its Importance @PHARMAVEN #cip #validation #pharmaven #cleaning
In Hindi, CIP Cycle, Cleaning in Place Cycle, Development, Validation #validation @PHARMAVEN
Cleaning And Sanitization of Classified Areas #USFDA @PharMaven #cleaning #sanitization #aseptic
Cleaning And Sanitization in Aseptic Area
How to Clean and Sanitize Classified Areas
Your Queries
1. How To Clean Classified Areas
2. How to Sanitize Classified Areas
USFDA Facing Audit- Facility Readiness and Site Round 👩💼🤵👩🏫👩⚖️👍👍👍
How to face FDA Audit-Facility Readiness, Site Round, #USFDA #GMP #pharma #audits @Dhavalkumar Surti
USFDA GMP Operational Excellence 🏌️🧘👩⚖️👩🏫🤵👩💼
My First Video on Operational Excellence where Importance of Procuring Correct Equipment and Defining Right Procedures, Qualifica...
Cleaning And Sanitization of Classified Areas #USFDA @PharMaven #cleaning #sanitization #aseptic
Cleaning And Sanitization in Aseptic Area
How to Clean and Sanitize Classified Areas
Your Queries
1. How To Clean Classified Areas
2. How to Sanitize Classified Areas
USFDA Facing Audit- Facility Readiness and Site Round 👩💼🤵👩🏫👩⚖️👍👍👍
How to face FDA Audit-Facility Readiness, Site Round, #USFDA #GMP #pharma #audits @Dhavalkumar Surti
USFDA GMP Operational Excellence 🏌️🧘👩⚖️👩🏫🤵👩💼
My First Video on Operational Excellence where Importance of Procuring Correct Equipment and Defining Right Procedures, Qualifica...
Просмотров: 556
Видео
In Hindi, PUPSIT As per EU ANNEX-1, Pre Use Post Sterilization Integrity Testing @PHARMAVEN
Просмотров 611День назад
PUPSIT What is PUPSIT as per EU ANNEX-1? #pharmaven #validation #qualification #sterile #eugmp कैसे 0.2 micron फिल्टर बैक्टीरिया को फिल्टर करता है? @PHARMAVEN #aseptic #filteration #bacteria Filter Validation, Bacterial Retention Test, Brief Understanding @PHARMAVEN #filter #bacterial How 0.2 Micron Filter retains Bacteria? @PHARMAVEN #filter #bacterial #usfda #aseptic #sterile Sterilizi...
Yield Calculation and Deviation Investigation @PHARMAVEN #pharmaven #yield #asepticprocessing
Просмотров 538День назад
Yield Calculation and Deviation Investigation #pharmaven #yield #asepticprocessing
What is Change Room Classification for Grade C B Areas @PHARMAVEN #pharmaven #qualification
Просмотров 469День назад
Change Room Classification for Grade C and Grade B Areas #pharmaven #qualification 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 Clea...
What is PUPSIT as per EU ANNEX-1? #pharmaven #validation #qualification #sterile #eugmp
Просмотров 84514 дней назад
PUPSIT What is PUPSIT as per EU ANNEX-1? #pharmaven #validation #qualification #sterile #eugmp कैसे 0.2 micron फिल्टर बैक्टीरिया को फिल्टर करता है? @PHARMAVEN #aseptic #filteration #bacteria Filter Validation, Bacterial Retention Test, Brief Understanding @PHARMAVEN #filter #bacterial How 0.2 Micron Filter retains Bacteria? @PHARMAVEN #filter #bacterial #usfda #aseptic #sterile Sterilizi...
What is Difference between oRABS and cRABS? @PHARMAVEN #pharmaven #hvac #validation #sterile
Просмотров 1,1 тыс.21 день назад
What is Difference between oRABS and cRABS? #pharmaven #hvac #validation #sterile 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...
Isolator and VHP cycle Validation #isolator @PHARMAVEN #vhp #validation #pharmaven #vhp #sterile
Просмотров 1,5 тыс.Месяц назад
Isolator and VHP cycle explanation, Validation #isolator #vhp
Risk Assessment for SIP of Filtration Vessel in Sterile Manufacturing #sterilization #validation
Просмотров 1 тыс.Месяц назад
Risk Assessment for SIP of Filtration Vessel in Sterile Manufacturing #sterilization #validation
In Hindi, Gowning Procedure for Aseptic Area #pharmaven #aseptic #validation #qualification #iso
Просмотров 1,2 тыс.2 месяца назад
Gowning Procedure for Aseptic Area #pharmaven #aseptic #validation #qualification #iso 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 ...
Gowning Procedure for Aseptic Area @PHARMAVEN #pharmaven #aseptic #validation #qualification #iso
Просмотров 4162 месяца назад
Gowning Procedure for Aseptic Area #pharmaven #aseptic #validation #qualification #iso 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 ...
4 Media Fill Failure English #aseptic #asepticprocessing @PHARMAVEN #mediafailure
Просмотров 3542 месяца назад
4 Media Fill Failure English #aseptic #asepticprocessing @PHARMAVEN #mediafailure
2 Media Fill Failure English @PHARMAVEN #asepticprocessing #validation #media #qualification #iso
Просмотров 1982 месяца назад
2 Media Fill Failure English @PHARMAVEN #asepticprocessing #validation #media #qualification #iso
2 Media Fill Failure Investigation English #asepticprocessing #validation #media #qualification
Просмотров 1512 месяца назад
2 Media Fill Failure Investigation English #asepticprocessing #validation #media #qualification
Media Fill Failure Investigation in English @PHARMAVEN #validation #aseptic #qualification #media
Просмотров 3882 месяца назад
Media Fill Failure Investigation in English @PHARMAVEN #validation #aseptic #qualification #media
Freeze Dryer Structure and working principle @PHARMAVEN #freezedrying #validation #qualification
Просмотров 9682 месяца назад
Freeze Dryer Structure and working principle @PHARMAVEN #freezedrying #validation #qualification
Which Tests to be done for Area Qualification?@PHARMAVEN #validation #qualification #ISO
Просмотров 4152 месяца назад
Which Tests to be done for Area Qualification?@PHARMAVEN #validation #qualification #ISO
Clean Room Qualification? @PHARMAVEN #qualification #validation #pharmaven #cleanroom #hvac #gmp
Просмотров 5692 месяца назад
Clean Room Qualification? @PHARMAVEN #qualification #validation #pharmaven #cleanroom #hvac #gmp
Can we Release Batch if Bulk is failing but Finish Product is Passing? @PHARMAVEN #pharmaven
Просмотров 1,1 тыс.3 месяца назад
Can we Release Batch if Bulk is failing but Finish Product is Passing? @PHARMAVEN #pharmaven
SAL and PNSU @PHARMAVEN #sal #pnsu #sterilization #validation #qualification #pharmaven #sterility
Просмотров 9113 месяца назад
SAL and PNSU @PHARMAVEN #sal #pnsu #sterilization #validation #qualification #pharmaven #sterility
SIP Validation #validation #qualification #pharmaven #sterilization #sip #sterile
Просмотров 2 тыс.3 месяца назад
SIP Validation #validation #qualification #pharmaven #sterilization #sip #sterile
Equilibration Time in Autoclave @PHARMAVEN #sterilization #validation #qualification #autoclave
Просмотров 1,3 тыс.3 месяца назад
Equilibration Time in Autoclave @PHARMAVEN #sterilization #validation #qualification #autoclave
Difference Between Pressure Gauge and Compound Gauge @PHARMAVEN #pharmaven #sterilization #gauge
Просмотров 1,1 тыс.3 месяца назад
Difference Between Pressure Gauge and Compound Gauge @PHARMAVEN #pharmaven #sterilization #gauge
Is Change Control required for SOP Revision when there is no change? #change #pharmaven #pharma
Просмотров 6863 месяца назад
Is Change Control required for SOP Revision when there is no change? #change #pharmaven #pharma
In English, Area Classification vs Guidelines Comparison @PHARMAVEN #validation #qualification
Просмотров 6084 месяца назад
In English, Area Classification vs Guidelines Comparison @PHARMAVEN #validation #qualification
Which Autoclave Load Items to Consider for Biological Indicator Placement? @PHARMAVEN #validation
Просмотров 6694 месяца назад
Which Autoclave Load Items to Consider for Biological Indicator Placement? @PHARMAVEN #validation
Area Classification and particle count limits in Different Guidelines @PHARMAVEN #validation
Просмотров 2,2 тыс.4 месяца назад
Area Classification and particle count limits in Different Guidelines @PHARMAVEN #validation
Autoclave Revalidation, All Load Patterns to Validate? @PHARMAVEN #autoclave #sterilization
Просмотров 7085 месяцев назад
Autoclave Revalidation, All Load Patterns to Validate? @PHARMAVEN #autoclave #sterilization
Media Fill for Terminal Sterilization Products? #validation #sterilization #media_fill @PHARMAVEN
Просмотров 8845 месяцев назад
Media Fill for Terminal Sterilization Products? #validation #sterilization #media_fill @PHARMAVEN
In English, Difference Between Validation and Qualification @PHARMAVEN #validation #qualification
Просмотров 6245 месяцев назад
In English, Difference Between Validation and Qualification @PHARMAVEN #validation #qualification
Difference Between Validation and Qualification @PHARMAVEN #validation #qualification #pharmaven
Просмотров 1,2 тыс.5 месяцев назад
Difference Between Validation and Qualification @PHARMAVEN #validation #qualification #pharmaven
Sir pls prepared one video on drug substance equipment related,
Sir make a video on B pharma student scope in production Sterile API plant
Best video ever ❤ thanks for sharing sir
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
Sir please explain about bubble point test use in filter integrity
Thank you
IV fluids bottle kyu sterilize karte hain
Very well explained sir
Dear Sir, Kindly provide information on what is ADS cy cycle in autoclave and difference between ADS and Bowie Dick ?
Wonderful information 👏 Thank you Sir
During autoclave.. pyrogens are killing or not plz tell me ……. if not then how it is not impacting on aur product plz tell me sir ..
Pyrogen not killed in autoclave but there is an allowed limit of BET in WFI, pure Steam which should meet and also limit for finished product BET which should meet
@@PHARMAVENthanks sir
Then why we are not sending vials from autoclave
We need completely dry vials which is difficult from autoclave Also it will make it a batch process and handling will be difficult Tunnel gives continuous supply of Depyrogenated vials hence preferred
Thanks sir
Thank you Sir
Sir Thank you very much for reaching my question clearing my doubt Thankyou you sir thank you very much
Sir ek media filling ke upar proper video
Already I have, refer below link हिंदी में: All About Media Fill in Aseptic Processing #media #aseptic @PHARMAVEN#usfda #sterile ruclips.net/video/OFnY_5Lfktg/видео.html
Sir autoclave ka qualification hota hai validation kyoki apne bataya hai ki validation process ka hota hai
Autoclave is qualified We validate sterilization process in autoclave
Great information sir Sir can you explain why there is need to do non viable particular count if we are already doing viable particular count
Area classification is determined basis non viable particle count and ISO 14644, EU Annex-1 and FDA Guidance for Industry September 2004 has defined limits for area classification in non viable particle counts. EU Annex I and FDA guidance also defines limit for viable count as well, which should meet during monitoring
Sir SCDM or TSB me kya different hai Ager dono ek hi hai to phir naam alag kyu hai??
Sir please make a video on different టైప్స్ ofairlocks
Sir jam ham nvpc karte hai to area grade a ,b c,d me kitne location pe nvpc karte hai Agra grade a me karte hai
Cnc area me dp nahi hota hai
Sir area qualification and area classification pe vodeo baniye
Area qualification karte kase hai
Ek sid build candation bhi hota hai
Duct leak limit kitna hai guidelines
Sir RLF kya hai and iska kam kya hai bataiye sir ispe video baniye
Good
Sir do isme cse kon sa use karenge
Nice information sir
Bataiye sir mai samjha nahi
D=1 sir kaise
Hindi me bna do ye video
Sir autoclave se relative question answer pe video banaiye for interview base
Re validation bhi hota hai
Yes When you make any change to process, vessel, API supplier etc then need to repeat process validation
Hindi pls
Nice information
What is slurry load
Sir disinfectant validation pe video banaiye sir
Your videos are very useful sir nice Pls give us this type of knowledge continuously so we can movitate our self and improve our knowledge. Thanks sir And sir one more question How to become auditor in pharma industry Like how to become auditor of usfda or mhrh of gmp?? Pls give some knowledge on it.
Sir thank you for sharing your knowledge 🙏
Upload video on lyophillzer ( freeze dry) n ALUS
Prepared video on the recovery study of laf,ahu,dpb
Sir very informative video, thank you. Kindly provide some details on F0, Fh l value, Spore log reduction, why Z value is 10 etc And how to ensure equipment are depyrogentaed after the autoclave cycle as they are only sterilized. Also recommended current guidelines to read. It will be very helpful sir🙏
There are some videos on my channel on topics you mentioned
I have videos on F0, D and Z value explanation
Sir,One video on Power failure's strategy
Very nice! Please also state the importance of the number of pulsating vacuum applications being included in the validation protocol.
Dear sir please inform new BMR agar bana ho tu uska liya kya step follow karna chahiye
❤
Thanku sir for such a informative video. Pls make video on filter integrity test like BPT, WIT, Diffusion test if possible.
Thank you very much sir
Very nice sir