Comparability for Biologics

Comparability for Biologics is a conference dedicated to testing strategies and practical approaches to determine comparability throughout all stages of development including:

• Tools for characterising and analysing change to a product (inc. biochemical and biophysical tools)
• Practical insight on regulation requests and CMC and considerations
• Applications of Quality by Design to montior/control process related impurity levels
• Analytical strategies for better product understanding
• Change implementation from early phase to post-license
• Heterogeous? Taking the next the step

Who should Attend

Heads of Department, Directors, Principle Scientists, Managers and Senior Scientists of: Analytical, Bioanalytical development, CMC, Regulatory affairs, Quality control, Development, Research and development, Quality assurance and Pre clinical development.