March 14, 2024 | 3:00 p.m. IST 

This exclusive online event consists of a session by Dr. Milind Bagul from Raptim Research and a panel discussion by industry experts. The event aims to provide a comprehensive overview of the latest guidelines and best practices in bioanalytical method validation, as outlined by the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH).

Discussion points:

• Understanding the significance and scope of the ICH M10 guidelines
• Interpretation of M10 guidelines for different experiments
• Discussion on experiment design and acceptance
• Requirement of additional experiments (if any)which are not covered in M10
• Harmonization of method validation experimental design all across Indian Pharma and CRO’s

Agenda

Speaker and panelists