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28 set 2017 ano - 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.

Adicionado na linha do tempo:

Opioids and the FDA

ByAnastasia
13 nov 2018
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0
521

Data:

28 set 2017 ano
Agora
~ 8 years ago
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