Brompheniramine hydrocodone and pseudoephedrine

Brompheniramine hydrocodone and pseudoephedrine

(b) With respect to a pharmaceutical product17-[2£L400that is subject to a patent, each Party shall make available an adjustment of the patent term to compensate the patent owner for unreasonable curtailment of the effective patent term as a result of the marketing approval process. 9.Each brompheniramine hydrocodone and pseudoephedrine Party shall disregard information contained in public disclosures used to determine if an invention is novel or buy phentermine diet pill has an inventive step if the public disclosure (a) was made or authorised by, or derived from, the patent applicant, and (b) occurs within 12 months prior to the date of filing of the application in the territory of the Party. 10.Each Party shall provide patent applicants with at least one opportunity to make amendments, corrections, and observations in connection with their applications. 400 17-[24] For Australia, the term pharmaceutical substance as used in Section 70 of the Patents Act 1990 on the brompheniramine hydrocodone and pseudoephedrine date of entry into force of this Agreement may be treated as synonymous with the term pharmaceutical product as used in this subparagraph. 11.Each Party shall provide that a disclosure of a claimed invention shall be considered to be sufficiently buy hydrocodone medical record without clear and complete if it provides information brompheniramine hydrocodone and pseudoephedrine that allows the invention to be made and used by a person skilled in the art, without undue experimentation, as of the filing date. 12.Each Party shall provide that a claimed invention is sufficiently supported by its disclosure if the disclosure reasonably conveys to a person skilled in the art that the applicant was in possession of the claimed invention, as of the filing date. 13.Each Party shall provide that a claimed invention is useful brompheniramine hydrocodone and pseudoephedrine if it has a specific, substantial, and credible utility. 14.Each Party shall endeavour to reduce differences in law and practice between their respective systems, including in respect of differences in determining the rights to an invention, the prior art effect of applications for patents, and the division of an application containing multiple inventions. In addition, each Party shall endeavour to participate in international patent harmonisation efforts, including the WIPO fora addressing reform and development of the international patent system. 15.Each Party shall endeavour to establish a cooperative framework between their respective patent offices as a basis for progress towards the mutual exploitation of search and examination work. 17.10: Measures related to certain regulated products 1. (a) If a Party requires, as a condition of approving the marketing of a new pharmaceutical product, the submission of undisclosed test or other data concerning safety or efficacy of the product, the Party shall not permit third persons, without the consent of the person who provided the information, to market the same or a similar product on the basis of that information, or the marketing approval granted to the person who submitted such information, for at least five years from the date of marketing approval by the Party.



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