Search results
Results from the WOW.Com Content Network
Until 2011, Quizlet shared staff and financial resources with the Collectors Weekly website. [13] In 2011, Quizlet added the ability to listen to content using text-to-speech. [14] In August 2012, it released an app for the iPhone and iPad and shortly afterward one for Android devices. [13]
[citation needed] For access to information at a given classification level, individuals must have been granted access by the sponsoring government organization at that or a higher classification level, and have a need to know the information. The government also supports access to SCI and SAPs in which access is determined by need-to-know.
The documentation required in an NDA is supposed to tell "the drug’s whole story, including what happened during the clinical tests, what the ingredients of the drug are, the results of the animal studies, how the drug behaves in the body, and how it is manufactured, processed and packaged.” [2] Once approval of an NDA is obtained, the new ...
An Abbreviated New Drug Application (ANDA) is an application for a U.S. generic drug approval for an existing licensed medication or approved drug.. The ANDA is submitted to FDA's Center for Drug Evaluation and Research, Office of Generic Drugs, which provides for the review and ultimate approval of a generic drug product.
One of the proposed NDAA bills for fiscal year 2015. On May 8, 2014, the House Armed Services Committee ordered the bill reported (amended) by a vote of 61-0. [10] The Committee spent 12 hours debating the bill and voting on hundreds of different amendments before voting to pass it. [11] 2016 National Defense Authorization Act for Fiscal Year 2016
[4] [page needed] [5] [6] [7] Congress has repeatedly resisted or failed to pass a law that generally outlaws disclosing classified information. Most espionage law criminalizes only national defense information; only a jury can decide if a given document meets that criterion, and judges have repeatedly said that being "classified" does not ...
The United States Food and Drug Administration's Investigational New Drug (IND) program is the means by which a pharmaceutical company obtains permission to start human clinical trials and to ship an experimental drug across state lines (usually to clinical investigators) before a marketing application for the drug has been approved.
A unilateral NDA (sometimes referred to as a one-way NDA) involves two parties where only one party (i.e., the disclosing party) anticipates disclosing certain information to the other party (i.e., the receiving party) and requires that the information be protected from further disclosure for some reason (e.g., maintaining the secrecy necessary to satisfy patent laws [5] or legal protection ...