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?
  • What is Potencymetry ?
  • How to do the calibration of potencymetry?    
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