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Who will certify clean room ok or notok
Thank you, simple and better explanation
not explain properly i don't understand that what you want to explain?0.5 =3520, 5 =29
Could you please explain how to calculate F0 value for autoclave validation
We have lab class iso 5 . The need of ach is 240 when i calculate it comes 14k cfm . Is there anyeay to reduce that? Any technec to achive the ach
Good video for pharma employee ....
Lecture is not properly delivered.
Grade A0.5@5 microns limit's tell me sir
Explanation is no well....
Thank u very much
Very nice explanation... Thanks
Under the area of LAF is known as grad A and it's surrounding area is known as Grade B
Your lacture is ok but u did not discribed that in sterile area how could identify that,this one A B C and D
Bagali ho kya
Roll: 75Description box Q2) Ans: Dispersed Oil Particulate(DOP)testing, also known as filter integritytesting, is the process in which the integrity of your HEPA (High EfficiencyParticulateAir) or ULPA (Ultra Low Penetration Air) filter is challenged through introducing particulates and measuring the output.
Q.2.Dispersed oil particulate(DOP) testing, also known as filter integrity testing, is the process in which the integrity of your HEPA (High EfficiencyparticulateAir) or ULPA (Ultra Low Penetration Air) filter is challenged through introducing particulates and measuring the output.
DOP (dispersed oil particulate) testing is the process in which the integrity of your HEPA (High Efficiency Particulate Air) or ULPA (Ultra Low Penetration Air) filter is tested through the introduction of particulates.With cleanrooms often protecting mission critical environments, filter integrity and efficiency is vital; HEPA filters are tested to 99.99% @ 0.3 micron efficiency with ULPA filters tested to 99.9995% @ 0.12 micron. During the DOP the whole filter face is tested to ensure that any damage or leak will be detected and located.Roll _79
Roll no-70Q.1.Cleanrooms are classified according to the cleanliness level of the air inside them. The cleanroom class is the level of cleanliness the room complies with, according to the quantity and size of particles per volume of air. The primary authority in the US and Canada is the ISO classification system ISO 14644-1. This standard includes the cleanroom classes ISO 1, ISO 2, ISO 3, ISO 4, ISO 5, ISO 6, ISO 7, ISO 8 and ISO 9, with ISO 1 being the cleanest and ISO 9 the dirtiest class (but still cleaner than a regular room). The most common classes are ISO 7 and ISO 8.
Roll: 75Description box Q1) Ans: Small numbers refer to ISO 14644-1 standards, which specify the decimal logarithm of the number of particles 0.1um or larger permitted per cubic metre of air. So, for example, an ISO class 5 clean room has at most 105-100,000 particles per metre cube.
Roll 69Q2. Ans:- Dispersed Oil Particulate (DOP) testing, also known as filter integrity testing,is the process in which the integrity of HEPA ( High Efficiency Particulate Air) or ULPA( Ultra Low Penitration Air) filter is challanged through introduction particulate and measuring the output.Oil is dispersed as an aerosol into the upstream flow of the filter media, while the number of particles in the down stream flow is measured using a calibrated protomrter.
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I want to buy this book... Can you help me out ? I have searched few e-commerce site. But didn't find it ..
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I request to youExplain all chapter one by onePls ma'am
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