Quality Control

Importance of Quality Contol in Pharmacetical Industry To make a Quality Medicines

Following are the useful articles on quality control management and analysis those are helpful to new as well as the experienced pharmaceutical professionals in quality improvement of products. This page is updated on a regular basis, therefore, don’t forget to visit again.

Step-by-Step Qulity Procedure Involved in Pharmacetical Manufacturing

• Common Causes of Low Quality in Pharmaceuticals
• In-Process Control Methods for the Active Pharmaceutical Ingredients Manufacturing
• Ultrasonic Cleaning for Equipment and Tooling
• Extraneous Peaks in Chromatographic Analysis
• 5 Major Differences between RO and EDI Water Systems
• Calibration Frequency of Instruments and Other Measuring Devices
• Requirements and Implementation of Continuous Training in Pharmaceuticals
• Why pH Value is Measured between 0 and 14?
• Quality by Design (QbD) in Pharmaceuticals
• Different Types of Titrations
• Computer System Validation in Pharmaceuticals
• Ghost Peaks in Chromatography: What They Are, Why You Should Be Aware of Them
• Different Types of HPLC Detectors
• Different Types of HPLC Columns Used in Analysis
• Steps for HPLC Method Development
• 10 Tips for HPLC Analysis In Pharmaceuticals
• Possible Causes of Out of Specification
• Mechanism of Separation of Components by HPLC
• How to Care for pH Meter Electrodes
• HPLC Column Void Volume
• Difference between Generic and Branded Medicines
• Quality Metrics for Pharmaceutical Manufacturing
• Steps for Analytical Method Development
• System Suitability in HPLC Analysis
• How Does Quality Cost Less in Long Term?
• What Does Quality Really Mean for Pharmaceuticals?
• Preparation of Molar and Normal Solutions
• Difference between GC and HPLC Techniques
• C18 HPLC Columns and Their Properties
• Difference between C8 and C18 Columns Used in HPLC System
• Differences between HPLC and UPLC
• Karl Fischer Reagent and Its Reactions
• Occupational Exposure Bands (OEBs) for Chemicals
• Difference between Sustained Release and Prolonged Release Tablets
• Climatic Zones for Stability Studies
• Different Types of Dissolution Apparatus
• Interview Questions for Quality Control / Assurance in Pharmaceuticals
• Difference Between Paddle and Basket Dissolution
• Forced Degradation Study in Pharmaceutical Stability
• Leak Detection of Colored Vials in Pharmaceuticals
• Mean Kinetic Temperature (MKT) in Stability Studies
• Analyst Qualification for Quality Control Laboratory
• What are symmetry and asymmetry?
• Qualification of Calculator
• Functions of Quality Control
• Difference between Quality Assurance and Quality Control
• Solvents used in HPLC Mobile Phase
• Difference between Incubator and BOD Incubator
• Checklist for Audit in Quality Control
• What is Delay Volume in HPLC?
• Impurity Profiling of Drug Substances in Pharmaceuticals
• Principle of HPLC (Liquid Chromatography)
• Principle of Bacterial Endotoxin Test (BET)
• Containers for Pharmaceutical Packaging
• Determination of Shelf Life of Solutions in Laboratory
• Principle of UV Spectrophotometer
• Working Principle of pH Meter
• Different Storage Conditions in Pharmaceuticals
• 5 Why Tool for Root Cause Analysis in Pharmaceuticals
• Protection of Light Sensitive Products
• FDA’s Data Integrity Issues in Indian Facilities
• User Requirement Specification (URS) of Equipments
• Calculation for Weighing Range of Balances
• SOP for Reduced Testing
• Process of Finding Impurities in Pharmaceutical Products
• Significant Change in Pharmaceutical Stability Testing
• Shelf Life Estimation of Pharmaceutical Products
• SOP for Password Policy and Data Backup and Storage for Computer Systems
• SOP for Safety in Laboratory
• Optical Activity in Pharmaceutical Analysis
• Tablet Dissolution Test in Different Stages (S1, S2 and S3)
• Sampling Plan SQRT n+1 (√n+1) for Pharmaceuticals
• Analytical Method Development Process for New Products
• Why Dissolution Test Apparatus Calibration with Salicylic Acid Tablets was Stopped?
• Instrument and Equipment List for Pharmaceuticals
• Color Codes for the Gas Cylinders in Pharmaceuticals
• Relative Response Factor (RRF) and its Calculation in HPLC Analysis
• Theoretical Plates ‘N’ and their Determination in HPLC Analysis
• Types and Size of Capsules
• Analytical Method Validation Protocol for Pharmaceuticals
• Difference Between Purified Water and De-mineralized Water
• Use of Ion Exchange Resins in Water Purification Systems
• Determination of Chemical Oxygen Demand of Wastewater
• Determination of Biological Oxygen Demand (BOD) in Waste Water
• Solid Pharmaceutical Dosage Forms – Capsules
• Oral Liquid Pharmaceutical Dosage Forms
• Difference Between Out of Specification and Out of Trend
• Good Laboratory Practices (GLP) Part-3
• Good Laboratory Practices (GLP) Part-2
• Good Laboratory Practices (GLP) Part-1
• High Performance Liquid Chromatography (HPLC)
• Determination of Total Organic Carbon in Purified Water
• Validation of Excel Calculation Sheets
• Guidelines for Pharmaceutical Stability Study
• Analytical Method Validation
• List of Glassware Used in Pharmaceuticals
• List of Chemicals and Media Required in Pharmaceuticals
• Principle and Calibration of Ultraviolet and Visible Absorption Spectrophotometry
• Analytical Method Validation Definitions in Pharmaceuticals
• SOP for Authorized Signatory
• SOP for Technology Transfer
• Calibration of Volumetric Glassware used in Pharmaceuticals
• SOP for Out of Trend (OOT)
• Guidelines for Receipt and Usage of Reference Standards and Qualification and Usage of Working Standards
• Method of Analysis for Vitamin E or Tocopheryl Acetate
• SOP for Operating Procedure of Water Bath
• SOP for Vortex Mixer
• Purified Water Testing in Pharmaceuticals
• SOP for Cleaning of Coulter Counter
• Sampling, Preservation and Storage Procedure of Water Sample
• SOP for Sampling and Testing Schedule of Purified Water
• SOP for Calibration of Autotitrator
• SOP for Calibration of pH Meter Temperature Sensor
• SOP for Calibration of HPLC Column Oven
• SOP for Calibration of HPLC (Low Pressure Quaternary Gradient Liquid Chromatograph)
• SOP for Linearity Check of High Performance Liquid Chromatograph (HPLC)
• SOP for Performance Checks of Karl Fischer Apparatus
• SOP for Performance Check of Autodiluter
• SOP for Calibration of Halogen Moisture Analyzer
• Difference Between Water (Moisture) Content and Loss on Drying (LOD)
• SOP for Verification of System Suitability Test Measured by Chromcard Software for GC
• SOP for Verification of System Suitability Test
• SOP for Calibration Procedure of U.V.Cabinet
• SOP for Performance Check of Karl Fischer
• SOP for Operational Check of Disintegration Test Apparatus
• SOP for Operational Check of Friability Test Apparatus
• SOP for Calibration of Hardness Tester
• SOP for Performance Check of UV/ Visible Spectrophotometer
• SOP for Cleaning of U.V. / Visible Spectrophotometer
• SOP for Calibration of Automatic Box Compression Strength Tester (Digital Model)
• SOP for Calibration of Melting Point Apparatus
• SOP for Performance Check of Automatic Distillation Apparatus
• SOP for Calibration of Conductivity TDS Meter
• SOP for Performance Check of Low Temperature Water Bath
• SOP for Method for Programme File Checks of Software of Instruments
• SOP for Calibration of Refractometer in Pharmaceuticals
• SOP for Calibration of Balance
• SOP for Calibration of Head Space Gas Chromatograph
• SOP for Calibration of Plunger Operated Pipette
• SOP for Performance Check of UV – Visible Spectrophotometer (Jasco)
• SOP for Calibration Total Organic Carbon (TOC) Analyzer
• SOP for Performance Check of Fourier Transform Infrared
• SOP for Calibration of Atomic Absorption Spectrophotometer (AAS)
• SOP for Calibration of Glassware in Pharmaceuticals
• SOP for Guideline for System Suitability Test for HPLC Analysis
• SOP for Calibration of Bursting Strength Tester
• SOP for Calibration of Coulter Counter
• SOP for Operational Qualification of Dissolution Tester
• SOP for Calibration of Conductivity Meter
• Rounding off Figures of Analytical Results
• SOP for Calibration of Gas Chromatograph
• SOP for Calibration of Infrared Moisture Balance
• SOP for Calibration of Karl Fischer Apparatus
• SOP for Calibration of Refractometer
• Resolution Factor, Tailing Factor, Theoretical Plates and Capacity Factor in HPLC
• SOP for Calibration of Infrared Spectrophotometer
• SOP for Calibration of Brook Field Viscometer
• SOP for Calibration of Disintegration Test Apparatus
• SOP for Calibration of High Performance Thin Layer Chromatography
• SOP for Check Suitability of Dissolution Test Apparatus
• SOP for Calibration of pH Meters
• SOP for Calibration of Mercury Filled Glass Thermometer
• SOP for Handling and Testing of Various Samples
• SOP for Gowning Procedure for Visitors in Quality Control
• Water Content Determination by Karl Fischer
• SOP for Handling and Testing of Inprocess Sample
• SOP for Cleaning of Autodiluter
• SOP for Cleaning of Halogen Moisture Analyzer
• SOP for Preparation and Handling of Primary Standard
• SOP for Cleaning of Dissolution Tester
• SOP for Cleaning of Metrohm Karl Fisher
• SOP for Cleaning of Disintegration Test Apparatus
• SOP for Cleaning of Friability Test Apparatus
• SOP for Receipt and Maintenance of Working Standards of API
• SOP for Collection and Storage of Retained Samples of Packaging Material
• SOP for Cleaning of Tablet Hardness Tester
• SOP for Collection and Storage of Retained Samples of Raw Material
• SOP for Cleaning of Melting Point Apparatus
• SOP for Handling and Control for Prohibited Items
• Limit Test for Arsenic in Pharmaceuticals
• SOP for Cleaning of Box Compression Strength Tester
• Determination of Refractive Index
• SOP for Cleaning of Automatic Distillation Apparatus
• Determination of Freezing Point
• Determination of Boiling Range or Temperature and Distillation Range
• Determination of Optical Rotation and Specific Optical Rotation
• SOP for Selection Criteria and Its Procedure before Dissolution Profile Study
• Testing Procedure (Method of analysis) for Acetates, Acetyl Groups and Alkaloids
• SOP for Routine Cleaning Verifictaion by TOC-SSM Method
• Rounding off Values In GMP Documents in Pharmaceuticals
• SOP for Logic for Giving Number to the Method for Analysis of Packaging Material
• SOP for Writing Method of Analysis for Packaging Material
• SOP for Cleaning of Tap Density Apparatus
• Requirements of Schedule L1 (Indian GLP) Good Laboratory Practice in Pharmaceutical
• SOP for Rounding off the Analytical Test Results
• SOP for Behavior in Quality Control Department
• SOP for De-aeration of Dissolution Media
• What is Loss on Drying? and Determination of Loss on Drying
• SOP for Cleaning of High Performance Liquid Chromatography (HPLC)
• SOP for Cleaning of Fourier Transform Infrared Spectrophotometer
• Testing Procedure (Method of analysis) for Sulphur in Organic Compounds, Tartrates and Thiosulphates
• SOP for Cleaning of Water Purification System
• SOP for Qualification of Vendors
• Determination and Acceptance limits of Uniformity of Content of Single-Dose Preparations
• SOP for Allocating Document Protocol Number for Instrument Qualification
• SOP for Retesting Schedule of Packaging Material
• Conductivity of Purified Water (Apparatus and Procedure) in Pharmaceutical
• SOP for General Test Procedure
• Determination of Ethanol-Soluble Extractive
• SOP for Cleaning Procedure of Balances
• SOP for Cleaning of Gas Chromatograph (Head Space)
• Determination of Zinc Content
• SOP for Disposal of Expired Chemicals, Reagents, Solvents and Micro-biological Medium
• Test for Free Formaldehyde (Formaldehyde Content)
• SOP for Cleaning of Centrifuge
• SOP for Cleaning of Bursting Strength Tester
• Identification test of Phenothiazines
• SOP for Cleaning of Polariscope
• Testing procedure (Method of analysis) for Bromides, Calcium Salts and Carbonates
• SOP for Cleaning of Quardrant Meter
• Limit Test for Heavy Metals in Pharmaceuticals
• Testing Procedure (Method of analysis) for Xanthines and Zinc Salts
• Ultraviolet and Visible Absorption Spectrophotometer (Apparatus and Calibration)
• SOP for Cleaning of Puncture Resistance Tester
• SOP for Careful Handling of Poisonous Chemicals
• Good Laboratories Practice (GLP) in Pharmaceuticals
• SOP for Cleaning of Vacuum Oven
• SOP for Cleaning of Ultrasonic Bath
• SOP for Calibration Programme
• SOP for Release of Finished Product
• SOP for Cleaning of Water Bath
• Uniformity of Weight of Single-Dose Preparations
• SOP for Raw Material Release
• SOP for Cleaning of Polarimeter
• SOP for Operation of Sampling Booth
• Method for Nitrite Titration
• SOP for Control of Master Data Generation by Computer System
• Raw Water Testing (Method of Analysis) as per IP/BP/USP
• Maintenance of Primary Standards in Pharmaceutical Industries
• Purified Water Testing (Method of analysis) as per IP/BP/USP
• Purified Water Specification as per IP/BP/USP
• SOP for Cleaning of High Performance Thin Layer Chromatograph
• SOP for Cleaning of Refractometer
• SOP for Use of Log Card for Equipment Status
• SOP for Cleaning of Brooke Field Viscometer
• SOP for Cleaning of Karl Fischer Apparatus
• Determination of Sulphur Dioxide
• SOP for Cleaning of U.V. /Visible Spectrophotometer
• Determination of Peroxide Value
• SOP for Cleaning Procedure for Dissolution Test Apparatus
• SOP for Cleaning of Atomic Absorption Spectrophotometer
• SOP for Sampling and Release of Raw Materials
• Guideline for Preparation of Mobile Phase Required for HPLC
• SOP for Retesting Schedule of Raw Material (For API)
• HPLC Column Performance Evaluation and Column Care
• SOP for Cleaning of Photoflurometer
• Size-Exclusion Chromatography
• Determination of Assay of Vitamin D
• Handling of Out of Calibration Instruments and Equipment
• SOP for Measurement of Particle Size of Raw Materials Using Microscopic Method
• SOP for Statistical Study for Trend Analysis of Purified Water and Water for Injection
• Determination of Weight Per Millilitre and Relative Density
• SOP for Allocating Identification Number to Instrument/Equipment
• Determination of Total Solids
• SOP for Sieve Analysis
• SOP for Issuance, Maintenance & Disposal of HPLC / GC Columns
• SOP for Action to be Taken for Unusual Observation for Instrument During Calibration
• Determination of Foreign Organic Matter
• SOP for Handling of the Spillages in the Laboratory
• Limit Tests in Pharmaceuticals
• Determination of Esters
• SOP for HPLC Column Receipt, Checking and Regeneration
• Determination of Saponification Value
• SOP for Retesting Schedule of Raw Material
• SOP for Evaluation of Analyst’s Performance
• Determination of Loss on Ignition
• SOP for Maintenance and Cleaning Procedure for Sampling Equipment
• SOP for Logic for Giving Number to the Method for Analysis of Finished Product and Raw Material
• Method of Analysis for Acetone
• SOP for Gowning Procedure for Quality Control
• Testing Procedure (Method of analysis) for Potassium Salts, Salicylates and Silicates
• SOP for Laboratory Cleaning
• SOP for Sampling of Raw Material
• SOP for Sampling of the Packaging Material
• SOP for Preparation of Volumetric Solutions
• Heavy Metals Testing
• SOP for Preparation of Bench Reagents
• SOP for the Preventive Maintenance of all Quality Control Instruments
• SOP for Storage and Use of Reagents & Chemicals
• SOP for Preparation and Handling of Working Standards
• Test for Sulphated Ash and Total Ash
• SOP for Manual Glassware Cleaning
• Identification Test of Barbiturates
• SOP for Washing of HPLC Column After Use
• Testing Procedure (Method of analysis) for Aluminium Salts, Amines and Ammonium Salts
• Melting Range or Temperature (Apparatus and Deternination)
• SOP for Handling & Usage of Hazardous Chemicals
• SOP for Destroying the Inprocess, Finished Product and Raw Materials Samples Timely After Testing
• pH Values (Apparatus and Method of Determination)
• SOP for Procurement and Handling of Reference Standard
• Disintegration Test and Apparatus
• Determination of Acid Value
• Testing Procedure (Method of analysis) for Benzoates, Bicarbonates and Bismuth Compounds
• Determination of Solubility in Pharmaceuticals
• Determination of Assay of Oxygen
• Testing Procedure (Method of analysis) for Ferric salts, Ferrous Salts and Iodides
• Dissolution Test and Apparatus
• Determination of Assay of Nitrous Oxide
• Paper Chromatography (Apparatus and Procedure)
• Testing Procedure (Method of analysis) for Mercury Compounds, Nitrates and Phosphates (Orthophosphates)
• Limit Test for Aluminium
• Testing Procedure (Method of analysis) for Chlorides, Citrates and Esters
• Testing Procedure (Method of analysis) for Silver Compounds, Sodium Salts and Sulphates
• Limit Test for Potassium and Sulphates
• Potentiometric Titration
• Powder Fineness (Types of Powder)
• Handling, Cleaning & Storage of Cuvettes of Spectrophotometer
• Testing Procedure (Method of analysis) for Antimony, Arsenic and Barium Salts
• Determination of Viscosity by Using Ostwald-type, Suspended-level and Rotating Viscometer
• Determination of Assay of Steroids
• SOP for Vacuum Test Apparatus
• Limit Test for Iron and Lead
• Contents Uniformity (Weight or Volume) of Packaged Dosage Forms
• Thin-Layer Chromatography (TLC Method and Apparatus)
• Principle and Calibration of TOC (Total Organic Carbon) Analyzer
• Testing Procedure (Method of Analysis) for Lactates, Lead Compounds and Magnesium Salts
• Determination of Nitrogen
• Preparation and Standardization of Volumeteric Solutions
• SOP for Material and Product Labeling in Production Area
• SOP for Calibration of Oven
• Update on Schedule L1
• Determination of Particle Size by Microscopy
• Determination of Unsaponifiable Matter
• SOP for Calibration of Thermometer
• SOP for Calibration of Dry Bath
• SOP for Training Procedure for Quality Control
• SOP for Testing of Miscellaneous Samples
• SOP for Calibration of pH Meter (GMPH)
• SOP for Calibration of pH Meter (pH Tutor)
• SOP for Calibration of Vacuum Oven
• Apparatus and Method for Fluorimetry
• SOP for Magnetic Stirrer with Hot Plate
• SOP for Bursting Strength Tester
• Determination of Iodine Value
• SOP for Centrifuge Machine
• Determination of Hydroxyl Value
• SOP for Sonicator
• Specification for Water for Injection (WFI) as per USP
• Flame Photometry (Apparatus and Method)
• SOP for Particle Counter
• Pharmaceutical Terms and Defination
• Appearance of Solution
• SOP for Handling of Reference and Working Standards
• Determination of Methoxyl Group
• SOP for Analyst Validation/ Qualification in Quality Control
• Congealing Range or Temperature
• Preparation and Standardization of 0.1 M Silver Nitrate
• Preparation and Standardization of 0.1 M Sodium Thiosulphate
• Determination of Acetyl Value
• Preparation and Standardization of 0.1 M Hydrochloric acid (HCl)
• Assay of Calcium Carbonate
• Preparation and Standardization of 0.1 N Perchloric acid
• Atomic Absorption Spectrometry
• SOP for Control of Record of Analysis in Quality Control
• SOP for Backup/Restore Analytical Data in Electronic Form
• Friability of Uncoated Tablets
• SOP for Recording of Analytical Data
• Assay of Calcium Citrate
• Assay of Ascorbic acid
• Preparation and Standardization of 0.1 M Disodium Edetate (EDTA)
• SOP for Safety in Quality Control
• SOP for Computer System Validation
• SOP for Good Laboratory Practice (GLP)
• SOP for Analysis and Release of Finished Product Sample
• Atomic Emission Spectrometry
• SOP for Calibration of Hot Air Oven
• SOP for Washing of HPLC Columns
• SOP for Control Environment Chamber (40 °C/75 % RH)
• SOP for Calibration of Potentiometric Titrator (Metrohm)
• SOP for Calibration of UV-Vis Spectrophotometer
• SOP for Calibration of Polarimeter
• SOP for Glassware Washing
• Calibration of Centrifuge Apparatus
• Calibration of Vernier Caliper
• Calibration of Refractometer
• Calibration of Brookfield Viscometer
• Calibration of Hardness Tester
• Calibration of Glassware (Class A and Class B)
• SOP for Calibration of Glassware
• SOP for Storage of Sampling Tools
• SOP for Preventive Maintenance of Instrument
• SOP for Sampling of Raw Material in Pharmaceuticals
• SOP for Calibration of FT-IR Spectrometer
• SOP for HPLC Analysis and Documentation
• SOP for Calibration of Vernier Caliper
• Analytical Balance Calibration (Updated)
• UV Cabinet Calibration in Pharmaceuticals
• Calibration of Karl Fischer Apparatus
• Calibration of Friability Test Apparatus
• Calibration of Viscometer
• Calibration of Dissolution Testing Apparatus
• HPLC Calibration Procedure
• SOP for Standard, General Reagents and Indicator Solutions
• SOP for Maintenance of Desiccator
• SOP for Cleaning of Quality Control Laboratory
• SOP for Muffle Furnace
• SOP for Cleaning of Refrigerator
• SOP for Operation and Cleaning of Hot Air Oven
• SOP for Handling of Glassware
• SOP for Cleaning of Sampling Equipment
• SOP for Tap Density Apparatus
• SOP for Operation and Calibration of pH Meter (Pico+)
• SOP for Milli-Q Water System from Milipore
• SOP for Operation and Calibration of Leak Test Apparatus
• SOP for UV Cabinet
• SOP for Melting Point Apparatus
• SOP for Operation and Calibration of Sieve Shaker
• SOP for Analysis on UV- Visible Spectrophotometer
• SOP for Refractometer
• SOP for Water Bath
• SOP for HPLC System Using Chemistation Software from Agilent
• SOP for Preparation and Standardization of Volumetric Solution
• SOP for Entry and Exit into Quality Control Laboratory
• Determination of Tapped Density
• Calibration of FTIR Spectrophotometer
• Calibration of Melting Point Apparatus
• Calibration of Gas Chromatography (GC)
• Indicator (Litmus Paper) and Test Papers
• Preparation and Standardization of 0.1 M Sodium Hydroxide
• Preparation and Standardization of 0.1 M Sulphuric Acid
• Preparation of Buffer Solutions
• Cleaning of Glassware with Nitric Acid and Chromic Acid
• Preparation and Standardization of 0.1 M Zinc Sulphate
• Preparation and Standardization of 0.1 M Zinc Chloride
• Preparation and Standardization of 0.1 M Tetrabutylammonium Hydroxide
• Preparation and Standardization of 0.1 M Titanium Trichloride
• Preparation and Standardization of 0.25 M Ethanolic Sulphuric Acid
• Preparation and Standardization of 0.1 M Sodium Nitrite
• Preparation and Standardization of 0.5 M Sulphuric Acid
• Preparation and Standardization of 0.1 M Sodium Methoxide
• Preparation and Standardization of 0.1 M Ethanolic Sodium Hydroxide
• Preparation and Standardization of 0.001 M Sodium Dodecyl Sulphate
• Preparation and Standardization of 0.02 M Potassium Permanganate
• Preparation and Standardization of 0.05 M Potassium Iodate
• Preparation and Standardization of 0.5 M Potassium Hydroxide in Ethanol (60 %)
• Preparation and Standardization of 0.1 M Ethanolic Potassium Hydroxide
• Preparation and Standardization of 0.1 M Potassium Hydroxide
• Preparation and Standardization of 0.0167 M Potassium Dichromate
• Preparation and Standardization of 1 M Nitric Acid
• Preparation and Standardization of 0.02 M Mercuric Nitrate
• Preparation and Standardization of 0.05 M Magnesium Sulphate
• Preparation and Standardization of 0.1 M Lithium Methoxide
• Preparation and Standardization of 0.1 M Lead Nitrate
• Preparation and Standardization of 0.05 M Iodine
• Preparation and Standardization of 0.5 M Methanolic Hydrochloric Acid
• Preparation and Standardization of 1M Hydrochloric Acid
• Preparation and Standardization of 0.1 M Ferrous Ammonium Sulphate
• Preparation and Standardization of 0.1 M Ferric Ammonium Sulphate
• Preparation and Standardization of 0.0005 M Dioctyl Sodium Sulphosuccinate
• Preparation and Standardization of 0.02 M Cupric Sulphate
• Preparation and Standardization of 0.1 M Ceric Ammonium Sulphate
• Preparation and Standardization of 0.1 M Ceric Ammonium Nitrate
• Preparation and Standardization of 0.05 M Bromine
• Preparation and Standardization of 0.004 M Benzethonium Chloride
• Preparation and Standardization of 0.05 M Barium Chloride
• Preparation and Standardization of 0.1 M Ammonium Thiocyanate
• Calibration of Disintegration Test Apparatus
• Dimensions of Hard Gelatin Capsule Shells
• SOP for Bursting Strength Tester
• Operating Procedure for Weighing Balances
• Retesting of Raw Materials Through SAP System
• Calibration of Total Organic Carbon Analyzer
• Calibration of Halogen Moisture Analyzer
• SOP for Vacuum Pump
• Calibration of Digital Polarimeter
• Ultrasonic Bath
• Sampling Procedure for Purified Water
• Operating Procedure for Dissolution Test (DT) Apparatus
• Calibration of UV / Visible Spectrophotometer
• Calibration of Automatic Potentiometric Titrator
• SOP for Out of Specification (OOS) for Pharmaceutical Results
• SOP for Leak Tester
• SOP for Operation and Maintenance of Water Purification System
• SOP for Analysis of Water
• SOP for Water Sampling
• SOP for Calibration and System Suitability of Total Organic Carbon (TOC) Analyzer
• SOP for Milliflex Water Filtration Unit
• SOP for Operation and Calibration of Mettler Toledo Analytical Balance
• SOP for Operation and Calibration of Conductivity Meter
• SOP for Operation and Calibration of pH Meter
• SOP for Handling of a Laboratory Incident
• SOP for Good Chromatography Practices
• Method of Analysis for Sucrose (Refined Sugar)
• Method of Analysis for Stearic Acid
• Method of Analysis for Starch
• Method of Analysis for Sodium Starch Glycolate
• Method of Analysis for Sodium Propyl Parabean
• Method of Analysis for Sodium Methyl Parabean
• Method of Analysis for Sodium Lauryl Sulphate
• Method of Analysis for Sodium Hydroxide
• Method of Analysis for Sodium Citrate
• Method of Analysis for Sodium Carbonate Anhydrous
• Method of Analysis for Sodium Benzoate
• Method of Analysis for Riboflavin
• Method of Analysis for Polyethylene Glycol
• Method of Analysis for Microcrystalline Cellulose
• Method of Analysis for Mannitol
• Method of Analysis for Maleic Acid
• Method of Analysis for Magnesium Stearate
• Method of Analysis for Magnesium Hydroxide
• Method of Analysis for Lithium Carbonate
• Method of Analysis for Kollodone
• Method of Analysis for Hypromellose Phthalate
• Method of Analysis for Hydroxypropyl Methylcellulose (HPMC) K100
• Method of Analysis for Folic Acid
• Method of Analysis for Ethyl Cellulose
• Method of Analysis for Dibutyl Phthalate
• Method of Analysis for Dibasic Calcium Phosphate Dihydrate
• Method of Analysis for Di Sodium Edetate
• Method of Analysis for Cross Povidone
• Method of Analysis for Cross Carmelose Sodium
• Method of Analysis for Copper Oxide
• Method of Analysis for Colloidal Silicon Dioxide
• Method of Analysis for Citric Acid Anhydrous
• Method of Analysis for Calcium Stearate
• Method of Analysis for Calcium Silicate
• Method of Analysis for Calcium Citrate
• Method of Analysis for Calcium Carbonate
• Method of Analysis for Ascorbic Acid
• Method of Analysis for Anhydrous Lactose
• SOP for Leak Seal Test Apparatus
• SOP for Preparation of Rejection Note
• SOP for Calibration of Pipettes, Burettes and Volumetric Flasks Used in Quality Control
• SOP for Preservation of Control Samples of Active Ingredients
• SOP for Operating and Cleaning of Distilled Water Unit
• SOP for Testing, Release or Rejection of Finished Product
• SOP for Trend Analysis
• SOP for Cleaning of Quality Control Dept. Throughout Working
• SOP for Planning for Analysis and Reporting of Results
• SOP for Sampling and Release of Inprocess Samples
• SOP for Operation of Karl Fischer Apparatus
• SOP for Sampling of Raw Water and Purified Water
• SOP for Laboratory Safety
• SOP for Preparation and Standardization of Volumetric Solutions
• SOP for Operation and Calibration of Tablet Disintegration Apparatus
• SOP for Operation and Calibration of Bulk Density Apparatus
• SOP for Operation and Calibration of Friability Test Apparatus
• SOP for Oven of Loss on Drying
• SOP for Ultrasonic Cleaner
• SOP for Cleaning and Disinfection
• SOP for Sampling of Packing Material
• SOP for Operating of Potentiometer
• SOP for Preparation of Stock Solution for Limit Test
• SOP for Re-analysis of Raw Material
• SOP for Collection and Storage of Control Sample
• SOP for Testing and Release/Rejection of Packing Materials
• SOP for Stability Studies of Finished Goods
• SOP for Destruction of Rejected Materials
• SOP for Cleaning of Glassware Used in Chemical Testing
• SOP for Preparation of Working Standards
• SOP for Preparation of Reagent Solution
• SOP for Testing and Release/ Rejection of Raw Material
• SOP for Calibration of Instruments in Production and Quality Contro