| Literature DB >> 24613178 |
Abstract
The EU regulation (EU 1901/2006 Paediatric Regulation) that entered into force in 2007 has changed the field of medicinal drug development for children in the EU. Five years after its implementation a large number changes due to this regulation have been incorporated by Pharmaceutical Industry considering the development of new candidate drug. This report is a review of changes already implemented and the aspects of paediatric drug development, which still needs to be addressed in future working in the fields to provide better medicines for children.Entities:
Keywords: Authorisation; Clinical trials; Drug development; European regulation; Paediatric medicines
Mesh:
Year: 2014 PMID: 24613178 DOI: 10.1016/j.ijpharm.2014.03.019
Source DB: PubMed Journal: Int J Pharm ISSN: 0378-5173 Impact factor: 5.875