21. Not until the regulatory committee meticulously reviewed the newly submitted clinical trial data ______ the pharmaceutical conglomerate to resume the production of its controversial medical device.
(A) they allowed
(B) did they allow
(C) the committee allowed
(D) was allowed
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統計: A(0), B(2), C(0), D(0), E(0) #4070164
統計: A(0), B(2), C(0), D(0), E(0) #4070164