Innovation and Patent Law Reform: Hearings Before the Subcommittee on Courts, Civil Liberties, and the Administration of Justice of the Committee on the Judiciary, House of Representatives, Ninety-eighth Congress, Second Session, on H.R. 3285, H.R. 3286, and H.R. 3605 Innovation and Patent Law Reform, March 28, April 26, and June 6, 27, 1984, 2. daļaU.S. Government Printing Office, 1985 - 2897 lappuses |
No grāmatas satura
1.–5. rezultāts no 100.
951. lappuse
... bill is as S. 255 and H.R. 6444 . based on the simple principle that only the earliest issued patent which either ... bill by a 2 to 1 majority of PMA members . not believe that the bill fairly addresses and solves the problem of ...
... bill is as S. 255 and H.R. 6444 . based on the simple principle that only the earliest issued patent which either ... bill by a 2 to 1 majority of PMA members . not believe that the bill fairly addresses and solves the problem of ...
984. lappuse
... bill ( H.R.3605 ) which will be before your subcommittee next week . As I mentioned , we have serious concerns with some provisions of this measure . Your willingness to hear from consti- tutional , law and patent experts is encouraging ...
... bill ( H.R.3605 ) which will be before your subcommittee next week . As I mentioned , we have serious concerns with some provisions of this measure . Your willingness to hear from consti- tutional , law and patent experts is encouraging ...
985. lappuse
... bill which : ( 1 ) Restores patent life lost to regulatory review for innovative drug products ; and ( 2 ) Accelerates the availability of safe and effective generic drug products . We are prepared to support a bill that addresses the ...
... bill which : ( 1 ) Restores patent life lost to regulatory review for innovative drug products ; and ( 2 ) Accelerates the availability of safe and effective generic drug products . We are prepared to support a bill that addresses the ...
986. lappuse
... bill . For most drugs , this does not permit FDA to request safety and effectiveness data other than bioequivalence data . In addition , the bill does not authorize rejection of an ANDA for most drugs on grounds of lack of safety or ...
... bill . For most drugs , this does not permit FDA to request safety and effectiveness data other than bioequivalence data . In addition , the bill does not authorize rejection of an ANDA for most drugs on grounds of lack of safety or ...
989. lappuse
... bill , Bolar is now completely reversed so that infringement may not be alleged prior to ANDA filing . This portion of the bill raises serious constitutional questions as it relates to the elimination of rights on patents that have ...
... bill , Bolar is now completely reversed so that infringement may not be alleged prior to ANDA filing . This portion of the bill raises serious constitutional questions as it relates to the elimination of rights on patents that have ...
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Bieži izmantoti vārdi un frāzes
103 prior art 1962 Amendments 2d Cir Adkins ANDA antitrust Appeals available as prior Bass beta blockers bill Bolar challenge successful challenged the validity Circuit claims Clemens clinical testing company/client Consent Judgment contract Corp costs Court decision decision or settlement decline defendant Dextrose diazepam disclosed disclosure district court effective patent electrolyte federal patent filed firms flurazepam grant Hoffmann-La Roche I.V. Solution impact industry Injection innovation invalid inventor Labs Lear doctrine legislation licensee estoppel licensor litigation manufacture ment monopoly NAME TRADE NAME NCEs NDAS APPROVED patent application patent infringement patent law Patent Office patent protection patent system patent term restoration patent validity period pharmaceutical plaintiff preliminary injunction prior art prior invention question reduced to practice regulation regulatory Roche royalties Section 103 prior Sodium Sodium Chloride statutory Stiffel subject matter Supp supra note Tablet tion trade secret Travenol United unpatented USPQ
Populāri fragmenti
1471. lappuse - A patent may not be obtained though the invention is not identically disclosed or described as set forth in section 102 of this title, if the differences between the subject matter sought to be patented and the prior art are such that the subject matter as a whole would have been obvious at the time the invention was made to a person having ordinary skill in the art to which said subject matter pertains.
1724. lappuse - The economic philosophy behind the clause empowering Congress to grant patents and copyrights is the conviction that encouragement of individual effort by personal gain is the best way to advance public welfare through the talents of authors and inventors in "Science and useful Arts.
1138. lappuse - ... described in a printed publication in this or a foreign country, before the invention thereof by the applicant for patent, or b. the invention was patented or described in a printed publication in this or a foreign country or in public use or on sale in this country, more than one year prior to the date of the application for patent in the United States, or c.
1285. lappuse - The several courts vested with jurisdiction of cases arising under the patent laws shall have power to grant injunctions according to the course and principles of courts of equity, to prevent the violation of any right secured by patent, on such terms as the court may deem reasonable...
1412. lappuse - A person shall be entitled to a patent unless: a. the invention was known or used by others in this country, or patented or described in a printed publication in this or a foreign country, before the invention thereof by the applicant for patent, or b.
1722. lappuse - The utility of this power will scarcely be questioned. The copyright of authors has been solemnly adjudged, in Great Britain, to be a right of common law. The right to useful inventions seems with equal reason to belong to the inventors. The public good fully coincides in both cases with the claims of individuals.
1437. lappuse - The specification shall contain a written description of the invention, and of the manner and process of making and using it, in such full, clear, concise, and exact terms as to enable any person skilled in the art to which it pertains, or with which it is most nearly connected, to make and use the same, and shall set forth the best mode contemplated by the inventor of carrying out his invention.
1412. lappuse - States, or (c) he has abandoned the invention, or (d) the invention was first patented or caused to be patented, or was the subject of an inventor's certificate, by the applicant or his legal representatives or assigns in a foreign country prior to the date of the application for patent in this country on an application for patent or inventor's certificate filed more than twelve months before the filing of the application in the United States...
1380. lappuse - In any action for infringement the defendant may plead the general issue, and having given notice in writing to the plaintiff or his attorney thirty days before, may prove on trial any one or more of the following special matters: First.
1498. lappuse - A trade secret may consist of any formula, pattern, device or compilation of information which is used in one's business, and which gives him an opportunity to obtain an advantage over competitors who do not know or use it.