EMA: Draft reflection paper on the use of methyl- and propylparaben as excipients in human medicinal products for oral use

The European Commission has decided to revise the \'Guideline on excipients in the label and package leaflet of medicinal products for human use (CPMP/463/00 Rev.1)\'. A concept paper on the need for such revision has been published in 2012(EMA/CHMP/SWP/888239/2011). Parabens used in medicinal products is one of the priorities among excipients under revision.

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