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13 C.F.R. § 121.108(e). Moreover, all claims of a patent issued following an intentional misrepresentation of small entity status may be held to be unenforceable as the result of inequitable conduct, i.e., fraud upon the United States Patent and Trademark Office. See MPEP § 2016; 37 C.F.R. § 1.27(h). As long as any small-entity assertions ...
The United States Patent and Trademark Office (USPTO) is an agency in the U.S. Department of Commerce that serves as the national patent office and trademark registration authority for the United States. The USPTO's headquarters are in Alexandria, Virginia, after a 2005 move from the Crystal City area of neighboring Arlington, Virginia.
In Madstad Engineering Inc. v. USPTO, Appeal No. 2013-1511 (Fed. Cir. July 1, 2014) plaintiff challenged the constitutionality of the act in placing an undue burden on its firm. Specifically, the plaintiff had to heighten computer security around potential inventions to prevent hackers from stealing intellectual property because of the first-to ...
Patent applications can be filed at the United States Patent and Trademark Office (USPTO). Prior to June 7, 1995, the duration of a US utility patent was 17 years from patent issuance. Since that date, the duration of the US utility patent is 20 years from the earliest effective filing date.
The following three lists of generic and genericized trademarks are: . marks that were originally legally protected trademarks, but have been genericized and have lost their legal status due to becoming generic terms,
In tandem, the Under Secretary is also the Director of the United States Patent and Trademark Office within the Commerce Department, filling dual roles. [1] The Under Secretary is appointed by the President of the United States, with the consent of the United States Senate, to serve at the pleasure of the President.
Drug innovators were given protections in two ways. First, a new kind of market exclusivity was introduced, by means of a new five-year period of data exclusivity awarded when the FDA approves marketing of a drug that is a new chemical entity; during that period the FDA cannot approve a generic version of the drug. [3]
Electronic Filing System of the United States Patent and Trademark Office (USPTO), also referred to as EFS-Web or simply EFS, was a web-based system for submitting patent applications and related documents electronically.