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Quizlet was founded in October 2005 by Andrew Sutherland, who at the time was a 15-year old student, [2] and released to the public in January 2007. [3] Quizlet's primary products include digital flash cards , matching games , practice electronic assessments , and live quizzes.
The authorization bill is the jurisdiction of the Senate Armed Services Committee and House Armed Services Committee and determines the agencies responsible for defense, establishes recommended funding levels, and sets the policies under which money will be spent. [3] The appropriations bill provides funds.
Prior to the roll-out of Python 3, projects requiring compatibility with both the 2.x and 3.x series were recommended to have one source (for the 2.x series), and produce releases for the Python 3.x platform using 2to3. Edits to the Python 3.x code were discouraged for so long as the code needed to run on Python 2.x. [10]
The Act provided that the FDA was entitled to collect a substantial application fee from drug manufacturers at the time a New Drug Application (NDA) or Biologics License Application (BLA) was submitted, with those funds designated for use only in Center for Drug Evaluation and Research (CDER) or Center for Biologics Evaluation and Research ...
The PDUFA date serves as a good first approximation of when a final decision on drug approval can be expected. Sponsors frequently publish PDUFA dates for their pending applications, [1] and while there is no official list of PDUFA dates, [10] several websites collect PDUFA dates from press announcements in a calendar form.
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 ...
In United States pharmaceutical regulatory practice, a Complete Response Letter (CRL), or more rarely, a 314.110 letter, is a regulatory action by the Food and Drug Administration in response to a New Drug Application, Amended New Drug Application or Biologics License Application, indicating that the application will not be approved in its present form. [1]
In 2011, the Python Packaging Authority (PyPA) was created to take over the maintenance of pip and virtualenv from Bicking, led by Carl Meyer, Brian Rosner, and Jannis Leidel. [ 10 ] With the release of pip version 6.0 (2014-12-22), the version naming process was changed to have version in X.Y format and drop the preceding 1 from the version label.