Paediatric Medicines: Formulation Considerations

Author:

Fátima Roque

Publisher

Heighten Science Publications Corporation

Reference28 articles.

1. 1. European Comission. Better Medicines for children. Proposed regulatory actions on paediatric medicinal products. 2002.

2. 2. European Parliament and Council of European Union. Regulation (EC) No. 1901/2006 of the European Parliament and of the Council of 12 December 2006 on Medicinal Products for Paediatric Use. Official Journal of the European Union. 2006.

3. 3. European Medicines Agency and Paediatric Committee. 10-year Report to the European Commission General report on the experience acquired as a result of the application of the Paediatric Regulation". 2016.

4. 4. Corny J, Lebel D, Bailey B, Bussieres JF. Unlicensed and Off-Label Drug Use in Children Before and After Pediatric Governmental Initiatives. J Pediatr Pharmacol Ther. 2015; 20: 316-328. Ref.: https://goo.gl/U6Rfrt

5. 5. Magalhaes J, Rodrigues AT, Roque F, Figueiras A, Falcao A, et al. Use of off-label and unlicenced drugs in hospitalised paediatric patients: a systematic review. Eur J Clin Pharmacol. 2015; 71: 1-13. Ref.: https://goo.gl/h9SJ3G

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