Description
Mastering Analytical Method Validation Training | Course
Become an expert in Analytical Method Validation with this comprehensive, industry-oriented training program designed as per ICH Q2 (R1/R2) guidelines. This course equips you with the knowledge and practical skills required to develop, validate, and document analytical methods used in pharmaceutical quality control and R&D laboratories.
Learn how to design regulatory-compliant validation protocols, execute studies with confidence, and generate accurate, audit-ready reports for global submissions.
Course Overview
Day 1, Session1
Analytical Method Validation, definition, Principle, chromatographic method classification, guidelines, Analytical Method Validation Parameters (definition & acceptance criteria)
Day2, Session 2
7-Step Analytical Method Validation Strategy, Necessary requirements to start Analytical Method Validation, How to define protocol for assay, related substances test, & content test with case study?
Day3, Session 3
How to perform Specificity, Detection limit (DL) & Quantitation limit (QL)? Case studies
Day 4, Session 4
How to perform Precision (System repeatability, Method repeatability, Intermediate precision & Method reproducibility)? Case studies
Day 5, Session 5
How to perform Precision Accuracy, Recovery, Linearity, Range & Relative response factor (RRF)? Case Study
Day 6, Session 6
How to perform Robustness & Stability of solutions? Case studies
Bonus Features
- Troubleshooting guides and common validation mistakes
- Regulatory insights and compliance tips
- Documentation templates and checklists
- Interview questions and expert recommendations
Who Should Attend?
- Analytical chemists and AR&D professionals
- QA/QC analysts and laboratory personnel
- Pharma R&D and quality professionals
- Students and freshers aiming for pharma careers
Why Choose This Course?
- Aligned with ICH Q2 and global regulatory expectations
- Practical, job-oriented training approach
- Real-time examples and industry case studies
- Enhances career opportunities in QC, QA, and R&D
Master the science of analytical method validation and build confidence to meet regulatory requirements, ensure data accuracy, and excel in pharmaceutical quality and compliance roles.
Sessions: 6 sessions (9 hours / 540 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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