The European Commission has launched a public consultation on the experience gained with the paediatric regulation. Until 28 November 2012 all interested citizens and public and private organizations are invited to send their contribution to this consultation to the European Commission.
The consultation builds on the European Medicines Agency's 'Five-year Report to the European Commission', which reflects on the experience acquired as a result of the application of the Paediatric Regulation.
The report summarises the areas of success and lessons learned of the implementation of the Paediatric Regulation since 2007 when it came into operation.
Between 2008 to 2011 13 new medicines as well as 30 new indications and 9 new pharmaceutical forms of existing medicines were authorised for use in children; these authorisations were made on the basis of Paediatric Investigation Plans (PIPs) agreed by the Agency's Paediatric Committee (PDCO).
An increasing number of ongoing clinical trials in children are conducted as part of an agreed PIP. By the end of 2011, the PDCO had adopted opinions on compliance for 29 agreed PIPs. This means that the full PIP was completed for these medicines. Full compliance with a PIP enables companies to request an extension of the duration of their patent for the medicine concerned. This is one of the main incentives of the Paediatric Regulation. National patent offices in 16 Member States granted a 6-month patent extension to 11 medicines, i.e. a total of 105 national Supplementary Protection Certificates (Article 36(1) of the Paediatric Regulation).