1. Regulation (EC) No. 1901/2006 of the European parliament and the council of 12th December 2006 on medicinal products for paediatric use http://ec.europa.eu/health/files/eudralex/vol-1/reg_2006_1901/reg_2006_1901_en.pdf
2. Guideline on the format and content of applications for agreement or modification of a paediatric investigation plan http://ec.europa.eu/health/files/eudralex/vol-1/2014_c338_01/2014_c338_01_en.pdf
3. Regulatory perspectives on acceptability testing of dosage forms in children;Kozarevicz;Int. J Pharm.,2014
4. Reflection paper: formulations of choice for the paediatric population http://www.ema.europa.eu/docs/en_GB/document_library/Scientific_guideline/2009/09/WC500003782.pdf
5. Guideline on the investigation of medicinal products in the term and preterm neonate http://www.ema.europa.eu/docs/en_GB/document_library/Scientific_guideline/2009/09/WC500003750.pdf