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Regulation (EC) No 1901/2006 on medicinal products for paediatric use & clinical research in vulnerable populations
Before any medicinal product is authorised for use in adults, it must undergo extensive pharmaceutical consistency and stability tests, toxicological tests and clinical trials to ensure that it is of high quality, safe and effective. The same approach may not always be applied to medicinal products...
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| Formato: | Texto |
| Lenguaje: | English |
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BioMed Central
2008
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2633263/ https://www.ncbi.nlm.nih.gov/pubmed/19063722 http://dx.doi.org/10.1186/1753-2000-2-37 |