The guidance provides a strategy to minimise the potential risk of medication errors associated with the introduction of high strength insulins (i.e. higher than the EU-wide standard of 100 units/ml concentration) and fixed combinations of insulin with another non-insulin injectable blood glucose lowering agent.
Consultation start date: 14/04/2015
Consultation end date: 14/06/2015
Posted on the EMA website on 14 April 2015
No hay comentarios:
Publicar un comentario