Rather, it is in line with a detailed investigation by the US Food and Drug and Administration (FDA).
The US Food and Drug Administration is expected to offer guidance in April about how the products should be regulated.
The US Food and Drug Administration (FDA) has approved the "morning-after" pill without a prescription for women aged 15 and over.
What happens then is up to the US Food and Drug Administration.
Some samples exceeded the "provisional total tolerable intake" (PTTI) set by the US Food and Drug Administration (FDA) by a factor of 120.
Some experts, though, warn against another commonly taken "cure" - paracetamol, which the US Food and Drug Administration says amplifies the effect on the liver.
Its submission to the US Food and Drug Administration to conduct the first trial in patients of human embryonic stem cells was the largest and most complex ever submitted.
Cephalon, the maker of Nuvigil, tried twice to get the drug officially approved to treat jet lag by the US Food and Drug Administration (FDA), the federal agency that regulates pharmaceutical companies.
Dr Richard Kalpit, the clinical reviewer at the US Food and Drug Administration, the US drugs regulator, who approved the drug, told the BMJ he was not given the data included in the documents.
Experience in the US of 69 deaths in 3.5 million Viagra prescriptions is not unexpected in the particular age group and the US Food and Drug Administration has not changed its view on the drug's safety.
The US Food and Drug Administration (FDA) approved Levitra, an orange pill compared to Viagra's blue, based on studies showing that men were on average five times more likely to achieve an erection suitable for intercourse when taking the pill compared with those given a dummy medicine.
This is already done in the US by the Food and Drug Administration.
Indeed, the results are positive enough that one leading pain expert in the US argues the Food and Drug Administration (FDA) should only license abuse resistant painkillers.
The US food regulator, the Food and Drug Administration (FDA), has just declared that transgenic AquAdvantage salmon have "no significant impact", which is usually the last step before the final approval.
The device is still not approved by the Food and Drug Administration in the US, and these trials, and others, are expected to last at least two or three years.
Geron has submitted a 22, 000 page submission to the Food and Drug Administration - the body which approves clinical trials in the US - the largest application on record.
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