Pharma Analytical Method Validation (ICH Q2)
Apply analytical method validation principles to meet regulatory expectations and prevent quality-related observations
Current Status
Not Enrolled
Price
₹100,000.00
This intensive training program on analytical method validation is designed for Quality professionals in the Pharma and Life Sciences sector. It addresses the challenge of non-compliant or insufficient method validation, which impacts regulatory approvals, inspections, and product lifecycle management. Participants will gain the ability to plan, execute, and assess analytical method validation in line with current regulatory expectations. The program uses regulatory guidelines–aligned validation scenarios and expert-led examples to ensure practical application.
Course Content
Meet Your Instructor
A pharmaceutical R&D professional with over 30 years of experience in small-molecule development, specializing in analytical development, quality control, and GMP-compliant operations. Proven expertise in operational governance, project management, risk assessment, and process improvement, with a strong track record of delivering efficiency-driven initiatives.
Extensive experience leading QC laboratories, including method setup, equipment calibration, preventive maintenance, and audit management. Successfully implemented a stage-gate process for new product development, reducing development timelines and improving productivity. Well-versed in global regulatory compliance across USFDA, TGA, WHO, MHRA, ANVISA, PMDA, and other major authorities.
Feedback & Reviews
₹100,000.00
This course includes:
- Learners 0 Students
- Lessons 4
- Topics 14
- Duration 6-17 Hours
- Quizzes 0
- Language English
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