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Controlled Substances Act - Wikipedia, the free encyclopedia
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A new drug application is first investigated by the "Main Board for Drug Registration" at the Ministry of Health. This Board decides if such a product is necessary for the Turkish pharmaceutical market. It comprises 20 members including physicians, pharmacists, chemists and biologists.
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Arguably, modest changes in the schedule of administration are unlikely to turn a good drug into a bad one (or vice versa), so refining the schedule might be considered a legitimate part of postlicensing drug development.
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Dawn Dearden with the Drug Enforcement Administration said: “At this point, it’s still a Schedule I drug, and we’re going to treat it as such.” The Food and Drug Administration declined to comment.
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Portland NORML's archive of drug policy news for Thursday, November 5, 1998. ... There are differences of opinion among some of us regarding drug policy but there are no differences in opinion that seriously ill patients should not mocked, even if one is "The largest newspaper in the Pacific Northwest".
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(8) For the purposes of subsection (5) and Schedule VIII, ... (3) If, under subsection (1), the court is satisfied of the existence of one or more of the aggravating factors enumerated in paragraphs (2)(a) to (c), but decides not to sentence the person to imprisonment, the court shall give reasons for that decision...
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Drug prohibition law - Wikipedia, the free encyclopedia
Drug prohibition law is prohibition-based law by which governments prohibit, except under licence, the production, supply, and possession of many, but not all, substances which are recognised as drug...
en.wikipedia.org/wiki/Drug_prohibition_law |
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