Because drainpoint is coolest point of autoclave and sterilization temprature should achieve till coolest point ,for ensuring that one temprature sensor is placed at drain point.thanks
@sanchalaldeshmukh2673
Жыл бұрын
Please share article on F0 value and log reduction
@msd6178
Жыл бұрын
It is very important information... Thank you sir
@PharmGrow
Жыл бұрын
Thanks
@AJ-rp9vg
Жыл бұрын
Many chances to contamination from drain point ,that's why require temperature sensor in drain for assure steam penetration achieve sterilization
@sanapathisekhar9780
Ай бұрын
Ans : to ensure Cold spot sterilization. Kudo to your piece of work 🤌🏾👌🏿👏🏿👏🏿. #valuable information.
@PharmGrow
Ай бұрын
Thank you so much 👍
@vmahendran269
Жыл бұрын
In drain point all water condensate drain in the point only so if temperature achieved in drain point all locations will be achieved normally
@PharmGrow
11 ай бұрын
Nice
@rajamoulicherala2199
Жыл бұрын
Drain point is cold point in autoclave chamber during sterilization
@madanprakash7445
7 күн бұрын
Some answers are incomplete or partly correct. In Autoclave BI used are spores of Geobacillus sterothermophilus because it is most temperature resistance organism in spore form
@PharmGrow
7 күн бұрын
Thanks for update 👍
@Kumar-sb3kd
2 ай бұрын
What is difference between standard cycle and HPHV cycle?
@PharmGrow
2 ай бұрын
There is no as such concept as standard cycle. Can you please explain for what you claim as standard cycle, so i can answer.
@pulavarthijanakiram9701
2 ай бұрын
Drain temperature point cold to Condensate temprature to forward stream line n cool water
@arun_108
Жыл бұрын
What is the reason for considering 6 log? Why not 5 log or 7 log? What is the significance of 6 log?
@PharmGrow
Жыл бұрын
Very good and expected question As we know that it is practically impossible to get 100 % assured on the sterilization process that it will Inactivate or kill all microorganisms. 6 log reduction means reducing microbial population of 1000000 (1 million) to 01 i.e. percent reduction of 99.9999. This is considered as very good % reduction for microbial population and recommended as a sterility assurance level (SAL) for sterilization processes. Hence, considering good percent reduction, 6 log reduction is accepted for sterility assurance level. With an overkill approach we can go beyond 6 log reduction i.e. 7, 8 and so on to have additional assurance. One more reason to go with 6 log reduction is to meet guideline requirements. Guideline reference: PDA’s technical report No.01 (revised 2007) recommends for 6 log reduction EPA performance standard of Hospital / Healthcare disinfection recommends for 6 log reduction for test organism. Hope this will help you.
@ahmadrasel6936
Жыл бұрын
Is it not required to perform I-Cold test (steam penetration) test everyday, sir??
@PharmGrow
Жыл бұрын
Yes. According to AAMI ( Association for the medical instrumentation ) bowie - dick test shall be conducted every day.
@Heliumvlogs
Жыл бұрын
In a worst condition is drain point to maintain temperature.. So it taken a main control feedback...
@PharmGrow
Жыл бұрын
Yes
@Manicstreams
Ай бұрын
What is the impact on pre and post loads if B& D test fails how you will assess it?
@RakeshKumar-sx8zm
Ай бұрын
If post vaccum phase is in running stage, during post vaccum phase gets low due to power interruption. Does it consider? Or Does it is under deviation? Cycle will be considered complete
@PharmGrow
Ай бұрын
It is deviation and cycle will be considered complete. Deviation has to be raised for root cause analysis and impact assessment likely drying of load.
@RakeshKumar-sx8zm
Ай бұрын
@@PharmGrow thanks for your information
@RakeshKumar-sx8zm
Ай бұрын
What is maximum length of silicone tube/ braided hose pipe in autoclave? As per FDA norms/ EN285 or other reference?
@PharmGrow
Ай бұрын
I need to check this. I will reply once i confirm
@rajeshpattnaik9480
Жыл бұрын
Drain sensor is placed due to which all others sensor temperature is being maintained
@PharmGrow
Жыл бұрын
Thanks 👍
@rajarao6563
Жыл бұрын
Very nice
@PharmGrow
Жыл бұрын
Thanks 👍
@jamalpurnareshjamalpurpark3532
Ай бұрын
Cold sopt
@sureshbabuyadla4049
Жыл бұрын
Why exposed biological indicators should incubate with in 4 hours. What is the rationale?
@PharmGrow
Жыл бұрын
To get accurate and reliable results exposed biological indicators should be incubate within 4 hours. Exposed biological indicators should be incubated within 4 hours to detect any surviving spores, assess the effectiveness of the sterilization process, and ensure accurate and reliable results in compliance with industry standards. Delay in incubation may allow allow other factors to act like temperature, oxygen etc. Hope you get answer. I searched for guideline reference but it was not found. We can follow this as standard industrial practice.
@shodhaharshad3043
Жыл бұрын
Sir in chemical indicater bacteria present or not ?
@PharmGrow
Жыл бұрын
Chemical indicators does not have bacteria present. It has chemical which undergoes physical or chemical change after sterilization process.
@shodhaharshad3043
Жыл бұрын
@@PharmGrow thanks sir
@msd6178
Жыл бұрын
Can please make a video about visual inspection qualification kit (Knap kit )
@PharmGrow
Жыл бұрын
Thanks for suggetion. This topic is already in my upcoming video list. You will get it very soon.
@msd6178
Жыл бұрын
Thank you sir... Please make it as early as possible....
@SudharaniReddycherla-cy4yj
Жыл бұрын
Sir 60 temperature daggara apali hot watertho appudu hot water off cheyyali reacterki
@PharmGrow
Жыл бұрын
Please translate in english.
@pritikagamit6714
9 ай бұрын
Sir, how can we know that we have achieved 6 log reduction.
@PharmGrow
9 ай бұрын
The concept of confirming 6 log reduction is very simple. We need not to perform testing for 6 log reduction after each routine / commercial cycle. We just need to perform validation of parameters (like temp, time and pressure) for sterilization cycle that it will achieve 6 log reduction. During cycle validation / revalidation only we need to prove with testing that set parameters are adequate to achieve 06 log reduction. For more detail info you can see my dedicated video on SAL i.e. sterility assurance level. You can get it in playlist of Injectable processing. Link given below, kzitem.info/news/bejne/0X9qvINjqaWLg3osi=LUTXBirId53AyC9I Hope this info will help you.
@jeshalsinhchavda575
Жыл бұрын
What is audit trail of KTA In QC...??
@PharmGrow
Жыл бұрын
It is as commonly referred i.e. sequence of recorded computer events that involves any activity around the operating system,applications or user actions.
@SaikumarGedam-o4w
5 ай бұрын
How many valves in Autoclave machine?
@PharmGrow
2 ай бұрын
It is based on make, model qnd design. It is not fix.
@satishthakur5742
Жыл бұрын
Autoclave ki validation video bnao
@PharmGrow
Жыл бұрын
Ok. I will prepare video on Autoclave Validation
@narasimhajogu3532
2 ай бұрын
Autoclave validation video send me
@pulavarthijanakiram9701
2 ай бұрын
Wt is kelvin
@PharmGrow
2 ай бұрын
The kelvin (abbreviation K), less commonly called the degree Kelvin (symbol, o K), is the Standard International ( SI ) unit of thermodynamic temperature.
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