Industrial Chemistry & Pharmaceutical Quality Control Training

Introduction

Analytical testing ensures the safety, purity, and potency of pharmaceuticals, food, environmental samples, and bioproducts.

Course Outline

Unit 1 - API & Formulation Characterization: Assay of Active Ingredient, Preservative Content Determination, Identification biochemical tests, Quantify active ingredients, verify raw material identity.
Unit 2 - Microbiological Quality Assurance: Determine antibiotic potency, Microbial Limit Test (MLT), Antibiotic Assay (Microbiological Assay), Sterility Testing.
Unit 3 - Pharmaceutical Product & Vitamin Analysis: Assay & Analysis of product, Analysis of Vitamin C, Estimation of Drug Content in Pharmaceuticals.
Unit 4 - High-Performance Liquid Chromatography (HPLC): Principle of HPLC, Parts, Detectors and Application, Standard Preparation, sample run and data analysis.
Unit 5 - Gas Chromatography (GC): Principle of Gas Chromatography, Parts, Detectors and Application, Standard Preparation, Sample run and data analysis.

Industrial Importance

Unit Details Technologies / Instrumentation
1 Formulation Characterization Pipetting, Preparation & pH, Biosafety & Waste Disposal
2 Microbiological Quality Assurance Microbial Analysis, Sterilization & Safety
3 Pharmaceutical Product Analysis Titration and Spectrophotometry
4 Analysis by HPLC HPLC with PDA and FLD Detector
5 Gas Chromatography Analysis Agilent Gas Chromatography System and Software

Application

Combination of chromatography (HPLC and GC) and microbiology forms the foundational infrastructure for product safety, regulatory compliance, and quality assurance of cosmetics, food, pharma and many industries.

Information

How does Analytical Testing & Chromatography training help your career?

Pharmaceutical QC teams need analysts skilled in assay validation, microbial limit testing, and chromatographic analysis. This training builds exactly those competencies, positioning you for QC/QA roles in pharma and analytical testing labs.

Which instruments will I use for pharmaceutical analysis?

You'll gain hands-on experience with HPLC and GC systems for compound analysis, along with microbiological assay techniques for sterility and antibiotic potency testing.

What is the duration of the training and the fee structure?

Duration: 80 Hrs or Up to 45 Days

Service Charges: We charge fee to cover the expenses of chemical and reagents that is  INR 12,000 /- (Indian Nationals) & $200 (Foreign Nationals)

Note: The program utilizes advanced instrumentation, specialized chromatographic resins, and high-grade analytical reagents. Because the fee directly covers these extensive consumable costs and dedicated instrument, the fee structure is fixed and non-negotiable.

Who is eligible to attend this training program?
  • The program is designed for undergraduate, postgraduate, and doctoral candidates (B.Sc., M.Sc., B.Tech, M.Tech, Ph.D.) in Biotechnology, Microbiology, Biochemistry, Life Sciences, Pharmacy, or Biochemical Engineering, as well as early-career industry professionals, QA/QC analysts, and academic faculty looking to upskill in bioprocessing

 

How do I download brochure and registration form?

Download Training Brochure: d

 

registration-form

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