Pharmaceutical Analytical Research Course | Training

8,100.00

Complete Pharmaceutical Analytical Research Course covering carrier, HPLC, GC, method development, validation (ICH), GMP, impurity profiling, and QC/AR&D training with hands-on experience.

Description

Complete Pharmaceutical Analytical Research Course |  Training

The Complete Pharmaceutical Analytical Research Course is a comprehensive, industry-focused training program designed to equip students and professionals with practical skills in analytical method development, validation, and regulatory compliance for pharmaceutical laboratories.

This course covers advanced analytical techniques such as HPLC, GC, LC-MS, GC-MS, UV-Vis, FTIR, and dissolution testing, along with hands-on exposure to real-world Quality Control (QC) and Analytical Research & Development (AR&D) environments.

Key Highlights of the Training Program

 Instrumental Analysis Techniques

Gain practical expertise in:

  • High-Performance Liquid Chromatography (HPLC)
  • Gas Chromatography (GC)
  • LC-MS / GC-MS
  • UV-Visible Spectroscopy
  • FTIR Analysis
  • Dissolution Testing Apparatus

Method Development & Validation (ICH Q2 Guidelines)

  • Development of robust analytical methods (HPLC & GC)
  • Validation parameters: accuracy, precision, specificity, linearity, robustness
  • Stability-indicating method development

Chiral Method Development

  • Separation of enantiomers
  • Chiral column selection and optimisation techniques

Analytical R&D (AR&D)

  • Impurity profiling and identification
  • Forced degradation studies
  • Stability testing as per ICH guidelines

Quality Control (QC) Practices

  • Raw material testing
  • Finished product analysis
  • Documentation and reporting standards

Regulatory Compliance & GMP Training

  • Good Laboratory Practices (GLP)
  • Good Manufacturing Practices (GMP)
  • Regulatory guidelines: WHO, USFDA, MHRA
  • Data integrity and audit readiness

Specialised Course Modules

  • Advanced Method Development Techniques
  • Method Validation Strategies
  • Chiral Analysis
  • Impurity Profiling & Degradation Pathways
  • Data Integrity & Compliance in Pharma Labs

Who Should Enroll?

  • BSc, MSc, B.Pharm, M.Pharm fresh graduates
  • Analytical chemists and professionals seeking career growth
  • QA/QC laboratory personnel
  • Candidates aspiring to work in pharmaceutical R&D and testing labs

Training Modes Available

  • Classroom (In-Person Training)
  • Online Instructor-Led Programs
  • Corporate / Industrial Training

Career Opportunities After Completion

This course prepares you for roles such as:

  • QC Analyst
  • AR&D Scientist
  • Method Development Analyst
  • Stability Study Analyst
  • Regulatory Compliance Associate

Why Choose This Course?

  • Industry-relevant curriculum aligned with global standards
  • Hands-on instrument training
  • Real-time case studies and lab exposure
  • Placement assistance (if applicable)
  • Certification recognised by the pharma industries

Note: This training program is offered in flexible formats, including classroom (in-person), online courses (Foundation, Most Popular, and Advanced levels), as well as customised corporate training solutions for organisations.

Sessions: 6 sessions (9 hours / 5400 minutes each)

Mode of Training: Online (via Google Meet)

Certificate: Yes, a certificate of completion will be provided

Money-Back Guarantee: 30-day money-back guarantee

Outcome:

  • Strong foundational knowledge
  • Clear career direction
  • Improved decision-making for advanced learning

Language: English

Instructor: Dr Pramod Kumar Pandey (PhD in Chemistry) | 31+ years of experience in global and Indian pharmaceutical industries

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