该专员将负责撰写标准的和方案特殊的测试程序，还有相应的测试报告，以及保存测试结果。
The Individual will be responsible for writing standard and trial specific test scripts, along with reporting and documenting testing results.
作为批准新上市的药物的一个标准程序，FDA将和药物开发公司撰写一个拉帕替尼的使用说明标签。
As is standard procedure with all new drug approvals, the FDA worked with the drug's manufacturer to compose the instruction labeling accompanying Tykerb.
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