...投票，投票结果为15:0，这次投票等同于获得FDA批准，但条件为Medtronic公司必须进 行一项长期的批准后研究(post-approval study)，以调查其安全性。
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Sledge和其他肿瘤专家看到这些研究成果后，对vemurafenib充满信心，认为该药有可能在本年度就获得FDA的批准。
Sledge and other cancer experts are confident that based on these study results, vemurafenib will almost certainly will get FDA approval this year.
在进公司后不久，他就开始作为“研究院主管”开始开展工作，负责在研究报告在对外发布之前的审阅和批准。
Shortly after arriving, he began working as a "supervisory analyst," vetting and approving research reports before they were disseminated to the public.
米索弗认为，鉴于这21名受试者中的20人此前接受FDA批准的治疗方法后均无效果，所以这一研究结果尤其值得重视。
Mithoefer considers the findings especially notable given that 20 of the 21 participants had previously failed to obtain relief from FDA-approved treatments.
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