Quality control involves, the analysis of a product at its different stages being manufactured in Pharmaceuticals. Their primary role involves testing and analyzing pharmaceutical products to ensure they meet established quality standards. Quality control professionals are responsible for sampling, analyzing raw materials, and analyzing finished pharmaceuticals. They use advanced equipment and testing methods to identify any deviations from quality parameters, ensuring that the drugs are safe for consumption.
The below articles help in understanding the different processes at different stages. All articles will be updated on a regular basis as per the updation from cGMP and Regulatory requirements.
- Top 10 Common Audit Findings in Pharmaceutical Manufacturing
- Top Asked Interview Questions Answer on HPLC, GC, IR, UV, Mass Spectroscopy
- Top Asked Dissolution Interview Questions with Expert Answers from Pharma Professionals
- Procedure for Handling of Deviations (SOP)
- Understanding Drug Product Assay and Potency
- Flow Injection Analysis (FIA) Overview
- Dissolution Test Apparatus / Types of DT Apparatus Methods and Medium
- 0.01 M Sodium Tetraphenylborate Preparation and Standardization
- 0.1 M Tetrabutylammonium Hydroxide Solution Preparation and Standardization
- Silica Based Column Cleaning, Regeneration and Storage
- Degassing of HPLC Mobile Phase: Why Its Done?
- 0.1 N Perchloric Acid Preparation and Standardization
- Preparation and Standardization of Potassium Permanganate
- 0.1 M Sodium Thiosulfate Preparation and Standardization
- 0.1 M KOH Solution Preparation and Standardization
- 0.1N Silver Nitrate (AgNO3) Solution Preparation and Standardization
- 0.1 M Silver Nitrate Solution Preparation and Standardization
- 0.1 M Sodium Nitrite Preparation and Standardization
- 0.05 M EDTA Solution Preparation and Standardization
- Preparation and Standardization of 0.05 M Iodine Solution
- Preparation and Standardization of 0.1 M Ceric Ammonium Sulphate
- Preparation and Standardization of 0.1 M Disodium Edetate (EDTA)
- How can I Prepare and Standardization 0.5 M Sulfuric acid
- 1.0 M Sulfuric Acid Solution- Preparation, Standardization, Reagents, Formula
- 0.1 M Sodium Hydroxide (NaOH), Preparation and Standardization
- Preparation and Standardization of 1 M Sodium Hydroxide Solution (NaOH)
- Preparation and Standardization of 1.0 M Hydrochloric Acid
- Quality Control Test for Secondary Packing Materials
- Autoclave Qualification Tests, Purpose, Procedure, and Acceptance Criteria
- Accelerated Stability Study; Different Guidelines
- Difference between HPLC and LCMS with Schematic diagram
- Limit Test for Lead: Principle, Reagent, Procedure and Observation
- Limit Test for Arsenic in Pharmaceutical Analysis
- Limit Test for Sulphate: Principle, Reaction, Procedure and Result
- Limit Test for Chloride
- Limit Test for Iron
- Limit test in Pharmaceuticals / inorganic chemistry
- List of Quality Control Equipment in Pharmaceuticals
- Various Types of HPLC Columns
- Methyl Orange indicator Preparation | How to make w/v Methyl Orange
- Preparation and Standardization of 0.1 N HCl
- Difference between Humidity and Relative Humidity
- Moisture Content and Loss On Drying (LOD) in Pharmaceuticals
- pH Meter | Principle, Calibration, and Working
- Good Laboratory Practice (GLP) in Pharmaceutical
- High-Performance Liquid Chromatography (HPLC)
- Injectable | Parenteral | Sterile Preparations, types, Standard test
- Tablet Friability Test Calibration and Specification
- Pharmaceutical Sampling, types, tools ( Guidelines)
- Vernier Caliper measurement and operation in Pharma
- Handling of Laboratory Incident in Pharma
- Calibration of UV-visible spectrophotometer
- User Requirement Specification (URS) in Pharmaceutical
- Autoclave Validation | Study on temperature Probes
- Disintegration Test Apparatus: Diagram, Principle, Types, Procedure, Calibration, Limit and Assembly
- Bowie Dick Test for Autoclave Validation
- Fumigation and Fogging in Pharmaceutical
- Types of Water in Pharmaceutical, Usage and Technique to Prepare