National Accreditation Board for Testing & Calibration Laboratories (NABL) is an autonomous society providing Accreditation (Recognition) of Technical competence of a testing, calibration, medical laboratory & Proficiency testing provider (PTP) & Reference Material Producer (RMP) for a specific scope
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Tuesday, 20 February 2018
Pharma Interview Questions
Can any deviation in to change in to change control?
What is the difference between humidity and relative humidity?
What should be the temperature and humidity for the tablet compression?
In stability testing if sagnificiant occur then what will be the aaction paln?
What do you mean by MKT ( Mean kinetic Temperature ) in stabiltiy?
What are the stability Zones and Stability Conduction ?
What is the difference between Vaccum Pressure and Vapor Pressure?
What do you men by Bracketing and mixturing in stability?
How to select HPLC Column In for a perticular product?
what are the composition of a C18 column?
what is the validitation , validitation protocal , validation Plan master?
what is the process validation ?
what is the limit of cleaning validitation?
What do you mean by MACO ?
What is NOEL ?
What is Recovery Factor?
How much the minimum recovery should be in a swab sampling?
What is the acceptance cretria for the detergent washing?
What do you mean by LOD and Water Content ?
What is the difference between LOD and Water Content ?
What is the differrence between Validation and Qualification ?
What is the disintegration Time of Coated Tablet?
What is the limit for Friability of Tablet?
What is the disintegration time for dispersable Tablet?
What is the difference between Calibration and Validation ?
What do you mean by Q+5 in dissolution ?
What is the disintegration time for Hard Galetin Capsule?
What is the limit of disintegration for Enteric Coated Tablet?
What should Be the sampling Point in dissolution Test?
Which will give more drugs Released Paddle or Basket in Dissolution ?
Tablet of which drugs are used in Dissolution Calibration ?
What is the difference between Drugs Purity and Drug Potency?
What shoud be the minimum Limit of Working Standard ?
What is the storage Condition for referance Standard?
How impurity is analysed in any Tablets?
Why we use the placebo in analysis?
What is the procedure to prepare to Placebo?
What is the difference between Method Validation and Method Varification ?
What is the technology Transfer and How it done ?
What are the step for Sterilization for DRY Powder Injection Facility (For Starting )?
What exepitent are used for dry powder Injection ?
What should be the LOD of Syrup?
How Can youn fix known and unknown Limit for any Drugs Substances?
What is the relstive response factor in Related Substance ?
How do we can choose HPLC and Gas Chromatogaphy For Sample Analysis?
Why 3X Sampling plan are implemented in process validation ?
What is the difference between temperaroy change control and deviation ?
Why we are use toluene for resolution in UV Clibration ?
What is the Photo Stability ?
What is the pooled Sample and why it is required for Dillution Test?
Why we use di sodium tetra for determination of factor in Karl Fischer Titration ?
What are the closely Monitor in Parameter in Stability Study?
What are the limit for LOD and LOQ?
why should we now dispatch the process material to export?
What is the formula for Karl Fischer Standardization ?
How we fix validity Period of a volumetric solution and resandardization Due Date?
How quantitative stability studies are done?
What do you mean by CAPA?
In Karl Fischer Standardization why we use disodium Tartarate?
What is the difference between deviation and Out of Specification ?
What is the difference between Mix-Up and Cross- Contamination ?
What is GMP, cGMP, and GLP?
How we can do the calibration of HPLC?
How Polarimeter is Calibrated?
What is the difference between Analytical method Validation and Analytical method Tranfer?
How malting Point Appratus is Calibrated ?
What is the differecnce between Polarimeter lamp and IR lamp?
What is the difference between sonication and homozinitation ?
What is the diifferernce between Uniformity and of content and content Uniformatiy as official Test for all tablets?
What is the limit of Uniformity of Content as per USP?
What is pH?
How we can do the calibration of pH?
What is COD ?
What Is BOD?
What are the Difference Between COD and BOD ?
How Much Temperature are required in Laboratory?
How many Types of Titration ?
How we can do the calibration of Refracto meter ?
What is conductivity ?
How we do the calibration of Conductivity ?
How many Temperature are required for BOD ? and why?
How to make Seeding Water in BOD?
How to Prepare Culture in BOD?
What are the principal of UV?
How to do the calibration of AAS?
What is Stability ?
What is SOP ?
How to Prepare the SOP ? What content are required in SOP?
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