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23 July 2012
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The US Food and Drug Administration (FDA) this week published a citizen petition denial to a group seeking to pre-emptively block the approval of a supplemental New Drug Application (sNDA) for Gilead
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16 July 2012
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The US Food and Drug Administration's (FDA) drug regulatory division announced the approval of a new indication for Gilead’s Truvada (emtricitabine/tenofovir disoproxil fumarate), making it the first
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