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Quality Control


Know how to Calibrate the pharmaceutical instruments, prepare and standardization of volumetric solutions, method of analysis of different tests.

  • Assay of Ascorbic acid
  • Assay of Calcium Carbonate
  • Assay of Calcium Citrate
  • Apparatus and Method for Fluorimetry
  • Atomic Absorption Spectrometry
  • Atomic Emission Spectrometry
  • Analytical Method Validation
  • Analytical Method Validation Definitions in Pharmaceuticals
  • Analytical Method Validation Protocol for Pharmaceuticals
  • Appearance of Solution
  • Bursting Strength Tester
  • Calibration of Automatic Potentiometric Titrator
  • Calibration of Brookfield Viscometer
  • Calibration of Centrifuge Apparatus
  • Calibration of Digital Polarimeter
  • Calibration of Disintegration Test Apparatus
  • Calibration of Dissolution Testing Apparatus
  • Calibration of FT-IR Spectrophotometer
  • Calibration of Friability Test Apparatus
  • Calibration of Gas Chromatography (GC)
  • Calibration of Glassware (Class A and Class B)
  • Calibration of Halogen Moisture Analyzer
  • Calibration of Hardness Tester
  • Calibration of Heating Block
  • Calibration of Karl Fisher Apparatus
  • Calibration of Melting Point Apparatus
  • Calibration of Micropipettes
  • Calibration of Microscope
  • Calibration of Refractometer
  • Calibration of TOC (Total Organic Carbon) Analyzer
  • Calibration of Total Organic Carbon Analyzer
  • Calibration of UV / Visible Spectrophotometer
  • Calibration of Vernier Caliper
  • Calibration of Viscometer
  • Calibration of Volumetric Glassware used in Pharmaceuticals
  • Paper Chromatography (Apparatus and Procedure)
  • Operating Procedure for Dissolution Test (DT) Apparatus
  • Melting Range or Temperature (Apparatus and Determination)
  • Method for Nitrite Titration
  • Method of Analysis for Acetone
  • Method of Analysis for Anhydrous Lactose
  • Method of Analysis for Ascorbic Acid
  • Method of Analysis for Calcium Carbonate
  • Maintenance of Primary Standards in Pharmaceutical Industries
  • List of Standard Operating Procedures (SOPs) in Quality Control (QC)
  • List of Current ICH Quality Guidelines for Stability
  • Limit Test for Aluminum
  • Limit Test for Arsenic in Pharmaceuticals
  • Limit Test for Heavy Metals in Pharmaceuticals
  • Limit Test for Iron and Lead
  • Limit Test for Potassium and Sulphates
  • Limit Tests in Pharmaceuticals
  • Ionising Radiation Sterilization
  • Identification Test of Barbiturates
  • Identification of Environmental Flora
  • Identification test of Phenothiazines
  • Heavy Metals Testing
  • Handling, Cleaning & Storage of Cuvettes of Spectrophotometer
  • Handling of Out of Calibration Instruments and Equipment
  • HPLC Chromatography Calibration Procedure
  • HPLC Column Performance Evaluation and Column Care
  • Guidelines for Receipt and Usage of Reference Standards and Qualification and Usage of Working Standards
  • Guideline for Preparation of Mobile Phase Required for HPLC
  • Guidelines for Pharmaceutical Stability Study
  • Friability of Uncoated Tablets
  • Good Laboratories Practice (GLP) in Pharmaceuticals
  • Good Laboratory Practices (GLP) Part-1
  • Good Laboratory Practices (GLP) Part-2
  • Good Laboratory Practices (GLP) Part-3
  • Flame Photometry (Apparatus and Method)
  • Disintegration Test and Apparatus
  • Dissolution Test and Apparatus
  • Dimensions of Hard Gelatin Capsule Shells
  • Difference Between Water (Moisture) Content and Loss on Drying (LOD)
  • Determination of Total Organic Carbon in Purified Water
  • Determination of Total Solids
  • Determination of Unsaponifiable Matter
  • Determination of Viscosity by Using Ostwald-type, Suspended-level and Rotating Viscometer
  • Determination of Weight Per Millilitre and Relative Density
  • Determination of Zinc Content
  • Determination of Iodine Value
  • Determination of Loss on Ignition
  • Determination of Methoxyl Group
  • Determination of Nitrogen
  • Determination of Optical Rotation and Specific Optical Rotation
  • Determination of Particle Size by Microscopy
  • Determination of Peroxide Value
  • Determination of Refractive Index
  • Determination of Saponification Value
  • Determination of Shelf Life of Solutions in Laboratory
  • Determination of Solubility in Pharmaceuticals
  • Determination of Sulphur Dioxide
  • Determination of Tapped Density
  • Determination of Esters
  • Determination of Ethanol-Soluble Extractive
  • Determination of Foreign Organic Matter
  • Determination of Freezing Point
  • Determination of Hydroxyl Value
  • Determination of Boiling Range or Temperature and Distillation Range
  • Determination and Acceptance limits of Uniformity of Content of Single-Dose Preparations
  • Determination of Acetyl Value
  • Determination of Acid Value
  • Determination of Assay of Nitrous Oxide
  • Determination of Assay of Oxygen
  • Determination of Assay of Steroids
  • Determination of Assay of Vitamin D
  • Contents Uniformity (Weight or Volume) of Packaged Dosage Forms
  • Conductivity of Purified Water (Apparatus and Procedure) in Pharmaceutical
  • Congealing Range or Temperature
  • Climatic Zones for Stability Studies
  • Cleaning of Glassware with Nitric Acid and Chromic Acid
  • Retesting of Raw Materials Through SAP System
  • Resolution Factor, Tailing Factor, Theoretical Plates and Capacity Factor in HPLC
  • Raw Water Testing (Method of Analysis) as per IP/BP/USP
  • Purified Water Testing (Method of analysis) as per IP/BP/USP
  • Purified Water Testing in Pharmaceuticals
  • Purified Water Specification as per IP/BP/USP
  • Procedure for Qualification of Vendors for Raw Material and Packaging Materials
  • Rounding off Figures of Analytical Results
  • Rounding off Values In GMP Documents in Pharmaceuticals
  • Sampling Procedure for Purified Water
  • Size-Exclusion Chromatography
  • UV Cabinet Calibration in Pharmaceuticals
  • UV Light Efficiency Test
  • Ultrasonic Bath
  • Ultraviolet and Visible Absorption Spectrophotometer (Apparatus and Calibration)
  • Uniformity of Weight of Single-Dose Preparations
  • Validation of Excel Calculation Sheets
  • Water Content Determination by Karl Fischer
  • WHO SOP list for Pharma Quality Control Cleaning
  • WHO SOP List for Pharma Quality Control Operations
  • WHO SOP List for Pharma Quality Control
  • Primary Standards used in Standardization of Volumetric Solutions
  • Principle and Calibration of Ultraviolet and Visible Absorption Spectrophotometry
  • Principle of HPLC ( Liquid Chromatography )
  • Potentiometric Titration
  • Powder Fineness (Types of Powder)
  • Preparation of Annual Product Review
  • Preparation of Buffer Solutions
  • Preparation of Indicator Solutions
  • Preparation of Standard Solutions
  • Test for Free Formaldehyde (Formaldehyde Content)
  • Test for Sulphated Ash and Total Ash
  • Testing Procedure (Method of Analysis) for Lactates, Lead Compounds and Magnesium Salts
  • Testing Procedure (Method of analysis) for Acetates, Acetyl Groups and Alkaloids
  • Testing Procedure (Method of analysis) for Aluminium Salts, Amines and Ammonium Salts
  • Testing Procedure (Method of analysis) for Antimony, Arsenic and Barium Salts
  • Testing Procedure (Method of analysis) for Benzoates, Bicarbonates and Bismuth Compounds
  • Testing Procedure (Method of analysis) for Chlorides, Citrates and Esters
  • Testing Procedure (Method of analysis) for Ferric salts, Ferrous Salts and Iodides
  • Testing Procedure (Method of analysis) for Mercury Compounds, Nitrates and Phosphates (Orthophosphates)
  • Testing Procedure (Method of analysis) for Potassium Salts, Salicylates and Silicates
  • Testing Procedure (Method of analysis) for Silver Compounds, Sodium Salts and Sulphates
  • Testing Procedure (Method of analysis) for Sulphur in Organic Compounds, Tartrates and Thiosulphates
  • Testing Procedure (Method of analysis) for Xanthines and Zinc Salts
  • Testing procedure (Method of analysis) for Bromides, Calcium Salts and Carbonates
  • Therapeutic Goods Administration (TGA) Guidelines - Australia
  • Thin-Layer Chromatography (TLC Method and Apparatus)
  • Preparation and Standardization of 0.004 M Benzethonium Chloride
  • Preparation and Standardization of 0.1 M Ceric Ammonium Nitrate
  • Preparation and Standardization of 0.0005 M Dioctyl Sodium Sulphosuccinate
  • Preparation and Standardization of 0.001 M Sodium Dodecyl Sulphate
  • Preparation and Standardization of 0.0167 M Potassium Dichromate
  • Preparation and Standardization of 0.02 M Cupric Sulphate
  • Preparation and Standardization of 0.02 M Mercuric Nitrate
  • Preparation and Standardization of 0.02 M Potassium Permanganate
  • Preparation and Standardization of 0.05 M Magnesium Sulphate
  • Preparation and Standardization of 0.05 M Barium Chloride
  • Preparation and Standardization of 0.05 M Bromine
  • Preparation and Standardization of 0.05 M Iodine
  • Preparation and Standardization of 0.05 M Potassium Iodate
  • Preparation and Standardization of 0.1 M Ammonium Thiocyanate
  • Preparation and Standardization of 0.1 M Ceric Ammonium Sulphate
  • Preparation and Standardization of 0.1 M Disodium Edetate (EDTA)
  • Preparation and Standardization of 0.1 M Ethanolic Potassium Hydroxide
  • Preparation and Standardization of 0.1 M Ethanolic Sodium Hydroxide
  • Preparation and Standardization of 0.1 M Ferric Ammonium Sulphate
  • Preparation and Standardization of 0.1 M Ferrous Ammonium Sulphate
  • Preparation and Standardization of 0.1 M Hydrochloric acid (HCl)
  • Preparation and Standardization of 0.1 M Lead Nitrate
  • Preparation and Standardization of 0.1 M Lithium Methoxide
  • Preparation and Standardization of 0.1 M Perchloric acid
  • Preparation and Standardization of 0.1 M Potassium Hydroxide
  • Preparation and Standardization of 0.1 M Silver Nitrate
  • Preparation and Standardization of 0.1 M Sodium Methoxide
  • Preparation and Standardization of 0.1 M Sodium Nitrite
  • Preparation and Standardization of 0.1 M Sodium Thiosulphate
  • Preparation and Standardization of 0.1 M Tetrabutylammonium Hydroxide
  • Preparation and Standardization of 0.1 M Titanium Trichloride
  • Preparation and Standardization of 0.1 M Zinc Chloride
  • Preparation and Standardization of 0.1 M Zinc Sulphate
  • Preparation and Standardization of 0.25 M Ethanolic Sulphuric Acid
  • Preparation and Standardization of 0.5 M Methanolic Hydrochloric Acid
  • Preparation and Standardization of 0.5 M Potassium Hydroxide in ethanol (60 %)
  • Preparation and Standardization of 0.5 M Sulphuric Acid
  • Preparation and Standardization of 1 M Nitric Acid
  • Preparation and Standardization of 1M Hydrochloric Acid
  • Preparation and Standardization of Volumeteric Solutions
  • pH Values (Apparatus and Method of Determination)
  • What is Loss on Drying ? and Determination of Loss on Drying
  • Activated Carbon Filter and Increase in Efficiency for Water System
  • Addresses of Indian Pharmaceutical Companies
  • An Overview of ISO 14644 Clean Room Classification
  • Analytical Balance Calibration
  • Biocontamination Control Techniques for Purified Water System
  • Biofilm and Its Formation in Water System
  • Buffer Area and Its Maintenance in Sterile Manufacturing Facility
  • Chemical Sanitization of RO Systems and Biofilm Removal
  • Chlorination and De-chlorination of Water System
  • Cleaning and Housekeeping Procedure in Pharmaceuticals
  • Common Ways to Avoid Making the Most Frequent GMP Errors
  • Concept of Revalidation in Pharmaceuticals
  • Current Good Manufacturing Practice (cGMP)
  • Determination of Biological Oxygen Demand (BOD) in Waste Water
  • Determination of Chemical Oxygen Demand of Wastewater
  • Difference among Calibration, Validation & Qualification
  • Difference Between Out of Specification and Out of Trend
  • Difference Between Purified Water and De-mineralized Water
  • Drugs & Cosmetics Act 1940
  • Effectiveness and Criteria to Replace the UV Lights
  • GMP Audit Check List- Equipment
  • GMP Audit Check List- Filling and Packaging
  • GMP Audit Check List- Personnel and Premises
  • GMP Audit Check List- Process Validation
  • GMP Audit Check List- Sanitation and Hygiene
  • GMP Audit Check List- Storage of Starting Materials
  • GMP Audit Check List- Water Supply System
  • GMP Audit Check List- Weighing and Dispensing
  • Good Documentation Practices (GDP) in Pharmaceuticals
  • Guide to Inspections of High Purity Water Systems
  • Hold Time Study of Cleaned Equipments
  • How to plan for a GMP audit in Pharmaceuticals?
  • Internal Audit or Self Inspection Defects and Regulatory Compliance Check List
  • International Health Regulatory Bodies
  • Major Audit Findings about Equipment and Instruments
  • Mix Up and Cross Contamination in Pharmaceutical Manufacturing
  • Non-sterile Process Validation in Pharmaceuticals
  • Now Ask Your Questions and Answer others' Questions on Pharmaguideline.com
  • Oral Liquid Pharmaceutical Dosage Forms
  • Organogram and Job Responsibilities in Pharmaceuticals
  • Parenteral Added Substances
  • Passivation of Purified Water System/ WFI System in Pharmaceuticals
  • Pharmaceutical Contamination and Its Control
  • Pharmaceutical Interview Questions - Quality (QA and QC)
  • Pharmaceutical Terms and Definition
  • Prevention of Cross - Contamination During Processing
  • Prevention of Cross - Contamination by HVAC in Pharmaceuticals
  • Prevention of Cross - Contamination in Pharmaceuticals
  • Principle of Hygrometer and Its Use in Pharmaceuticals
  • Proposed Changes in ISO 14644-1
  • Prospective Validation
  • Purified Water Storage and Distribution System
  • Purified Water System
  • Purified Water System Validation
  • Purpose of Process Validation in Pharmaceuticals
  • Qualification of Systems and Equipments in Pharmaceuticals
  • Requirements of Schedule L1 (Indian GLP) Good Laboratory Practice in Pharmaceutical
  • Reverse Osmosis (RO) System for Water Purification
  • Role and Calculation of Air Changes per Hour in Clean Room Area
  • Sampling, Preservation and Storage Procedure of Water Sample
  • Schedule M
  • Separate Manufacturing Facility is Required for Manufacturing of Penicillin and Non-penicillin Products
  • Skill Matrix - Evaluation of Training in Pharmaceutical
  • Solid Pharmaceutical Dosage Forms - Capsules
  • Solid Pharmaceutical Dosage Forms - Tablets
  • Specification for Water for Injection (WFI) as per USP
  • Summary of ISO 14644 (ISO Cleanliness Classes)
  • Terminology & Definitions in Pharmaceuticals
  • Three Consecutive Batches for Validation in Pharmaceuticals
  • Tooling of Oral Solid Dosage Form (Tablet)
  • Top 10 Indian Pharmaceutical Companies on the Basis of their Net Profit
  • Types of Water used in Pharmaceutical Processes
  • Update on Schedule L1
  • Use of Ultra-Violet Light for Disinfection
  • Validation in Pharmaceutical Manufacturing
  • Validation of Shelf Life for 70% v/v Isopropyl Alcohol (IPA)
  • Validation Protocol for Efficacy of Chemical Disinfectants
  • Water for Injection (WFI) System Validation Process
  • What is HEPA filter? Its Use in Pharmaceuticals
  • What WHO says about cross-contamination?
  • WHO Guidelines for Pharmaceuticals
  • cGMP Guidelines for Pharmaceutical Industries Part-1
  • cGMP Guidelines for Pharmaceutical Industries Part-2
  • cGMP Regulations for Finished Pharmaceuticals and Medical Devices
  • Wastewater Treatment Process (Effluent Treatment)
  • WHO: Water for Pharmaceutical Use
  • Why 70% Isopropyl Alcohol is used as Disinfectant in Pharmaceuticals?



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