ICH Guidelines & Regulatory Compliance Training

ICH Guidelines & Regulatory Compliance Training

A specialized program designed to provide practical understanding of international regulatory requirements governing pharmaceutical development and manufacturing.

Topics Covered

  • ICH Q7, Q8, Q9 and Q10 Guidelines
  • Good Manufacturing Practices (GMP)
  • Data Integrity Requirements
  • Documentation Best Practices
  • Deviation and CAPA Management
  • Regulatory Inspection Readiness
  • Quality Risk Management

Benefits

  • Improved Compliance Culture
  • Regulatory Inspection Readiness
  • Better Documentation Practices
  • Reduced Compliance Risks

Join For Training

Date : 30 August 2026

Time : 10:00 AM - 01:00 PM


Registration Fee : ₹500