01.10.2015 - 02.10.2015
Nearing a decade of the EU Paediatric Regulation, with close to 2,000 submitted Paediatric Investigation Plans (PIPs), paediatric needs are recognised as an integrated part of drug development, with the inclusion of children now accepted as standard procedure. However, challenges remain, which can result in delayed access by children to innovative medicines. This paediatric conference will focus on ways to overcome these challenges, such as through collaboration, extrapolation, modelling & simulation and adaptive pathways. This is the conference to interact with EMA paediatric coordinators, Paediatric Committee (PDCO) members and other stakeholders interested in paediatric drug development. Patients’ and Healthcare professional’s views will complement the reports of practical experience.
Contact: DIA – Drug Information Association