Clean Room in injectable classification sterile pharmaceutical industry interview questions answers

  Рет қаралды 5,808

PharmGrow

PharmGrow

Күн бұрын

Clean Room in injectable / sterile pharmaceutical industry I 24 Interview questions and answers
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Questions covered:
Q. What is clean room ?
Q. What is limit for airborne particle concentration i.e. NVPC in Grade A, B, C and D ?
Q. What is maximum action limits for viable particle contamination ?
Q. Whether sinks and drains are allowed in Grade A and grade B area?
Q. What should be the air velocity in Grade A ?
Q. What are the methods for monitoring of viable and non viable particles ?
Q. What is use of air locks in clean room ?
Q. Where should be the hand washing facility provided in injectable manufacturing facility?
Q. What is the differential pressure requirement for adjacent rooms in clean area ?
Q. Whether view glasses and cameras shall be available in clean rooms ?
Q. What is requirement for Airflow patterns in cleanrooms for injectable dosage forms ?
Q. What are the requirements for door airlocks as per EU GMP Annex-1?
Q. When we should perform Glove integrity test for Gloves used in clean rooms ?
Q. In case of Isolator based facility what should be the background environment ?
Q. Which tests shall be covered in clean room classification ?
Q. What is Gowning Qualification for clean rooms?
Q. What is critical zone in clean rooms?
Q. Whether we need to define alert level and action level for non-viable particle count ?
Q. Which activities shall be performed in Grade A and Grade B ?
Q. Which activities shall be performed in Grade C and Grade D ?
Q. Whether conveyor belt can pass through Grade A to Grade B area?
Q. What is requirement for tubing’s used for NVPC counting ?
Q. Which type of monitoring's are commonly done in clean rooms of pharmaceutical industry ?
Q. Which guidelines are commonly referred for clean room classification in pharmaceutical industry ?
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Keywords to find this video:
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Пікірлер: 6
@vijay18panneer
@vijay18panneer Жыл бұрын
Super bro... kindly make for temperature mapping for storage area/ cold chamber from initial qualification to re-qualification and frequency with guidlines reference.
@PharmGrow
@PharmGrow Жыл бұрын
Sure. I will do it
@virendrajagtap4123
@virendrajagtap4123 Ай бұрын
Please give 1 hours seminar on Annexe 1 with complete changes
@PharmGrow
@PharmGrow Ай бұрын
Ok. I will prepare 👍
@virendrajagtap4123
@virendrajagtap4123 Ай бұрын
@@PharmGrow really thanks
@madanprakash7445
@madanprakash7445 27 күн бұрын
I feel the diameter of NVPC tubing is wrongly mentioned as 15 cm instead of 15 mm, please check
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