Development regulatory affairs for Oncology Medicinal Products 2015
27 Oct 2015
Online Event
Key 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
Past Events
Development regulatory affairs for Oncology Medicinal Products 2015 - 27 Oct 2015, Online Event (54567)
Development regulatory affairs for Oncology Medicinal Products 2026
Important
Please, check "Development regulatory affairs for Oncology Medicinal Products" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Medical device, Medical laboratories, Pharma
