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2. Danger Hiptop - Wikipedia

   en.wikipedia.org/wiki/Danger_Hiptop

   T-Mobile USA release followed two days later, on November 7, 2007. [13] It was later released in the UK and Germany by T-Mobile (as opposed to the Sidekick LX only being released by T-Mobile USA). The Sidekick/Hiptop Slide offers the same features and services as every other Danger device and an update to Danger's latest OS version (4.0).

3. Freedom Mobile - Wikipedia

   en.wikipedia.org/wiki/Freedom_Mobile

   The mid-range Smart and high-end Genius plans lost their names and had some features altered. Only SMS messages sent to Canadian numbers were included, and all MMS or non-Canadian SMS became pay-per-use. The Wind 25 plan included 100 MB of mobile Internet access, while the Wind 40 plan featured 5 GB of full-speed mobile Internet instead of ...

4. John Legere - Wikipedia

   en.wikipedia.org/wiki/John_Legere

   Prior to joining T-Mobile US, he was CEO of Asia Global Crossing from February 2000 to January 2002, and CEO of Global Crossing from October 2001 to October 2011 where he led the organization through bankruptcy and eventually an acquisition by Level 3 Communications.

5. Yelp - Wikipedia

   en.wikipedia.org/wiki/Yelp

   Users can give a review a "thumbs-up" rating, which will cause it to be ranked higher in the review listings. [95] Each day a "Review of the Day" is determined based on a vote by users. [96] According to The Discourse of Online Consumer Reviews many Yelp reviewers are internet-savvy adults aged 18–25 or "suburban baby boomers". [179]

6. Partisan Review - Wikipedia

   en.wikipedia.org/wiki/Partisan_Review

   Partisan Review (PR) was a left-wing small-circulation quarterly "little magazine" dealing with literature, politics, and cultural commentary published in New York City. The magazine was launched in 1934 by the Communist Party USA–affiliated John Reed Club of New York City and

7. Design review (U.S. government) - Wikipedia

   en.wikipedia.org/wiki/Design_review_(U.S...

   Design review is also required of medical device developers as part of a system of design controls described in the US Food and Drug Administration's governing regulations in 21CFR820. In 21CFR820.3(h), design review is described as "documented, comprehensive, systematic examination of the design to evaluate the adequacy of the design ...