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.
- Relative Response Factor (RRF) and its Calculation in HPLC Analysis
- Steps for HPLC Method Development
- Steps for Analytical Method Development
- User Requirement Specification (URS) of Equipments
- Why is Analytical Method Validation Required?
- Possible Causes of Out of Specification
- How to Care for pH Meter Electrodes
- What Does Quality Really Mean for Pharmaceuticals?
- 5 Why Tool for Root Cause Analysis in Pharmaceuticals
- Difference between C8 and C18 Columns Used in HPLC System
- 10 Tips for HPLC Analysis In Pharmaceuticals
- 4 Steps to Effective Change Control in Pharmaceuticals
- System Suitability in HPLC Analysis
- Different Types of HPLC Detectors
- Working Principle of pH Meter
- GMP Requirements in Pharmaceuticals
- Out of Specification Investigation in Pharmaceuticals
- Pharmaceutical Compliance and Product Quality
- Tips for Hazardous Chemical Handling in Laboratory
- The Shape of Pharmaceutical Dosage Forms
- Limitations and Advances in Dissolution Testing in Pharmaceuticals
- Non-conformance in Pharmaceuticals and Ways to Prevent it
- Improving Quality Through Supplier Audits in Pharmaceuticals
- 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
- Difference Between Paddle and Basket Dissolution
- Instrument and Equipment List for Pharmaceuticals
- Color Codes for the Gas Cylinders in Pharmaceuticals
- Use of Ion Exchange Resins in Water Purification Systems
- Why Dissolution Test Apparatus Calibration with Salicylic Acid Tablets was Stopped?
- Handling of Out of Calibration Instruments and Equipment
- Principle and Calibration of TOC (Total Organic Carbon) Analyzer
- 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
- pH Value, pH Scale and Its Measurement between 0 and 14
- Quality by Design (QbD) in Pharmaceuticals
- Checklist for Audit in Quality Control
- Principle and Calibration of Ultraviolet and Visible Absorption Spectrophotometry
- Calibration of Volumetric Glassware used in Pharmaceuticals
- 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)
- 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
- Calibration of FTIR Spectrophotometer
- Calibration of Melting Point Apparatus
- Calibration of Gas Chromatography (GC)
- Calibration of Disintegration Test Apparatus
- Calibration of Total Organic Carbon Analyzer
- Calibration of Halogen Moisture Analyzer
- Calibration of Digital Polarimeter
- Calibration of UV / Visible Spectrophotometer
- Calibration of Automatic Potentiometric Titrator
- 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 Reduced Testing
- SOP for Password Policy and Data Backup and Storage for Computer Systems
- SOP for Safety in Laboratory
- SOP for Authorized Signatory
- SOP for Technology Transfer
- SOP for Operating Procedure of Water Bath
- SOP for Sampling and Testing Schedule of Purified Water
- SOP for Vortex Mixer
- SOP for Cleaning of Coulter Counter
- 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
- 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 High Performance Liquid Chromatography (HPLC)
- SOP for Cleaning of Fourier Transform Infrared Spectrophotometer
- SOP for Cleaning of Water Purification System
- SOP for Qualification of Vendors
- SOP for Allocating Document Protocol Number for Instrument Qualification
- SOP for Retesting Schedule of Packaging Material
- SOP for General Test Procedure
- SOP for Cleaning Procedure of Balances
- SOP for Cleaning of Gas Chromatograph (Head Space)
- SOP for Disposal of Expired Chemicals, Reagents, Solvents and Micro-biological Medium
- SOP for Cleaning of Centrifuge
- SOP for Cleaning of Bursting Strength Tester
- SOP for Cleaning of Polariscope
- SOP for Cleaning of Quardrant Meter
- SOP for Cleaning of Puncture Resistance Tester
- SOP for Careful Handling of Poisonous Chemicals
- 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
- SOP for Raw Material Release
- SOP for Cleaning of Polarimeter
- SOP for Operation of Sampling Booth
- SOP for Control of Master Data Generation by Computer System
- 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
- SOP for Cleaning of U.V. /Visible Spectrophotometer
- SOP for Cleaning Procedure for Dissolution Test Apparatus
- SOP for Cleaning of Atomic Absorption Spectrophotometer
- SOP for Sampling and Release of Raw Materials
- SOP for Retesting Schedule of Raw Material (For API)
- SOP for Cleaning of Photoflurometer
- 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
- SOP for Allocating Identification Number to Instrument/Equipment
- 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
- SOP for Handling of the Spillages in the Laboratory
- SOP for HPLC Column Receipt, Checking and Regeneration
- SOP for Retesting Schedule of Raw Material
- SOP for Evaluation of Analyst’s Performance
- 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
- SOP for Gowning Procedure for Quality Control
- SOP for Laboratory Cleaning
- SOP for Sampling of Raw Material
- SOP for Sampling of the Packaging Material
- SOP for Preparation of Volumetric Solutions
- 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
- SOP for Manual Glassware Cleaning
- SOP for Washing of HPLC Column After Use
- SOP for Handling & Usage of Hazardous Chemicals
- SOP for Destroying the Inprocess, Finished Product and Raw Materials Samples Timely After Testing
- SOP for Procurement and Handling of Reference Standard
- SOP for Vacuum Test Apparatus
- SOP for Material and Product Labeling in Production Area
- SOP for Calibration of Oven
- 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
- SOP for Magnetic Stirrer with Hot Plate
- SOP for Bursting Strength Tester
- SOP for Centrifuge Machine
- SOP for Sonicator
- SOP for Particle Counter
- SOP for Handling of Reference and Working Standards
- SOP for Analyst Validation/ Qualification in Quality Control
- SOP for Control of Record of Analysis in Quality Control
- SOP for Backup/Restore Analytical Data in Electronic Form
- SOP for Recording of Analytical Data
- 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
- 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
- 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
- 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
- SOP for Bursting Strength Tester
- SOP for Vacuum Pump
- 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 Handling of a Laboratory Incident
- 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 Control
- 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 Columns Used in Analysis
- Mechanism of Separation of Components by HPLC
- HPLC Column Void Volume
- Difference between Generic and Branded Medicines
- Quality Metrics for Pharmaceutical Manufacturing
- How Does Quality Cost Less in Long Term?
- Preparation of Molar and Normal Solutions
- Difference between GC and HPLC Techniques
- C18 HPLC Columns and Their Properties
- Differences between HPLC and UPLC
- Karl Fischer Reagent and Its Reactions
- Occupational Exposure Bands (OEBs) for Chemicals
- Sustained Release and Prolonged Release Tablets and their Difference
- Climatic Zones for Stability Studies
- Different Types of Dissolution Apparatus
- Interview Questions for Quality Control / Assurance in Pharmaceuticals
- 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
- 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
- Different Storage Conditions in Pharmaceuticals
- Protection of Light Sensitive Products
- FDA’s Data Integrity Issues in Indian Facilities
- Calculation for Weighing Range of Balances
- Process of Finding Impurities in Pharmaceutical Products
- Significant Change in Pharmaceutical Stability Testing
- Shelf Life Estimation of Pharmaceutical Products
- 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
- 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
- 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
- Analytical Method Validation Definitions 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
- Purified Water Testing in Pharmaceuticals
- Sampling, Preservation and Storage Procedure of Water Sample
- Difference Between Water (Moisture) Content and Loss on Drying (LOD)
- Rounding off Figures of Analytical Results
- Resolution Factor, Tailing Factor, Theoretical Plates and Capacity Factor in HPLC
- Water Content Determination by Karl Fischer
- Limit Test for Arsenic in Pharmaceuticals
- Determination of Refractive Index
- Determination of Freezing Point
- Determination of Boiling Range or Temperature and Distillation Range
- Determination of Optical Rotation and Specific Optical Rotation
- Testing Procedure (Method of analysis) for Acetates, Acetyl Groups and Alkaloids
- Rounding off Values In GMP Documents in Pharmaceuticals
- Requirements of Schedule L1 (Indian GLP) Good Laboratory Practice in Pharmaceutical
- What is Loss on Drying? and Determination of Loss on Drying
- Testing Procedure (Method of analysis) for Sulphur in Organic Compounds, Tartrates and Thiosulphates
- Determination and Acceptance limits of Uniformity of Content of Single-Dose Preparations
- Conductivity of Purified Water (Apparatus and Procedure) in Pharmaceutical
- Determination of Ethanol-Soluble Extractive
- Determination of Zinc Content
- Test for Free Formaldehyde (Formaldehyde Content)
- Identification test of Phenothiazines
- Testing procedure (Method of analysis) for Bromides, Calcium Salts and Carbonates
- 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)
- Good Laboratories Practice (GLP) in Pharmaceuticals
- Uniformity of Weight of Single-Dose Preparations
- Method for Nitrite Titration
- 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
- Determination of Sulphur Dioxide
- Determination of Peroxide Value
- Guideline for Preparation of Mobile Phase Required for HPLC
- HPLC Column Performance Evaluation and Column Care
- Size-Exclusion Chromatography
- Determination of Assay of Vitamin D
- Determination of Weight Per Millilitre and Relative Density
- Determination of Total Solids
- Determination of Foreign Organic Matter
- Limit Tests in Pharmaceuticals
- Determination of Esters
- Determination of Saponification Value
- Determination of Loss on Ignition
- Method of Analysis for Acetone
- Testing Procedure (Method of analysis) for Potassium Salts, Salicylates and Silicates
- Heavy Metals Testing
- Test for Sulphated Ash and Total Ash
- Identification Test of Barbiturates
- Testing Procedure (Method of analysis) for Aluminium Salts, Amines and Ammonium Salts
- Melting Range or Temperature (Apparatus and Deternination)
- pH Values (Apparatus and Method of Determination)
- 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
- Limit Test for Iron and Lead
- Contents Uniformity (Weight or Volume) of Packaged Dosage Forms
- Thin-Layer Chromatography (TLC Method and Apparatus)
- Testing Procedure (Method of Analysis) for Lactates, Lead Compounds and Magnesium Salts
- Determination of Nitrogen
- Preparation and Standardization of Volumeteric Solutions
- Update on Schedule L1
- Determination of Particle Size by Microscopy
- Determination of Unsaponifiable Matter
- Apparatus and Method for Fluorimetry
- Determination of Iodine Value
- Determination of Hydroxyl Value
- Specification for Water for Injection (WFI) as per USP
- Flame Photometry (Apparatus and Method)
- Pharmaceutical Terms and Defination
- Appearance of Solution
- Determination of Methoxyl Group
- 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
- Friability of Uncoated Tablets
- Assay of Calcium Citrate
- Assay of Ascorbic acid
- Preparation and Standardization of 0.1 M Disodium Edetate (EDTA)
- Atomic Emission Spectrometry
- Determination of Tapped Density
- 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 (Phosphate, Acetate and other Buffers)
- 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
- Dimensions of Hard Gelatin Capsule Shells
- Operating Procedure for Weighing Balances
- Retesting of Raw Materials Through SAP System
- Ultrasonic Bath
- Sampling Procedure for Purified Water
- Operating Procedure for Dissolution Test (DT) Apparatus
- 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
