Development regulatory affairs for Oncology Medicinal Products 2015

Topics

• Knowledge of the main guidelines
• Understand how development in oncology is different
• Knowledge of faster approval pathways

Who should Attend

• Clinical trial associates
• Regulatory Affairs Personnel
• Personnel in the pharmaceutical and biotech industries who need a thorough understanding of the regulatory issues involved in the development of new medicinal products within the European Union Individuals who are seeking to update their knowledge of recent regulatory changes and their impact on product development
• Clinical operations personnel