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28 Sept 2017 Jahr - 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.
Zugefügt zum Band der Zeit:
Opioids and the FDA
By
Anastasia
13 Nov 2018
0
0
521
Datum:
28 Sept 2017 Jahr
Jetzt
~ 8 years ago
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