Manufacturing of Biologics and Biosimilars 2015 covers topics such as:
- Regulatory Requirements
- CMC Introduction Materials-Manufacturing-Control
- Critical Process Parameters and In- Process Controls for DS-Manufacture
- Overview Drug Substance-Manufacture
- CPPs and IPCs for DP-Manufacture
- Overview Drug Product-Manufacture
- Case Studies on Good Manufacturing Practice
- Statistics in Manufacturing
- Discussion and Q&A Session
Manufacturing of Biologics and Biosimilars 2015 brings together Directors, Vice Presidents, Managers, Heads and Scientists involved in:
- Biosimilars
- Biologics
- Biotechnology
- Biobetters
- Analytical Science
- Biotherapeutics
- Research & Development
- Process Science
- Quality Assurance
- Regulatory Compliance
- Intellectual Property
- Quality Control
- Scientific Affairs
- Clinical Immunology
- Portfolio planning
- Business Development
- Pharmacovigilance
- Legal Affairs
