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28 sett 2017 anni - FDA sent letters to IR opioid analgesic manufacturers informing them that their products that are intended to be used in the outpatient setting will be subject to the same REMS requirements as the ER/LA opioid analgesics.

Aggiunto al nastro di tempo:

Opioids and the FDA

ByAnastasia
13 nov 2018

Data:

28 sett 2017 anni
Adesso
~ 6 years and 8 months ago
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