Результаты (
английский) 2:
[копия]Скопировано!
a complete protocol for the examination of these specifications was followed using samples of the finished product diluted with the suggested infusion media and tested for 48 hours in order to to exhibit the compatibility of the product product.
According to the the Note of Guidance on Pharmaceutical Development the EMEA / The CHMP / 167068/2004 - section 2.6 "the info should cover the recommended in use shelf- life, at the recommended storage temperature and at the likely extremes of concentrations".
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