IP Applications definition

IP Applications means any applications for the registration of patents, copyright, designs, semi-conductor layout designs, trade names, trade marks, service marks, and any other intellectual property rights registration relating to Research IP;
Sample 1Sample 2Sample 3
IP Applications all applications filed with a Governmental Entity to obtain any Registered Intellectual Property, including applications for Patents, copyright registrations or Trademark registrations.
Sample 1Sample 2

Examples of IP Applications in a sentence

  • The Consortium shall treat the content of all Limited Exclusivity Agreements, Restricted Use Agreements and IP Applications as confidential.

  • The CGIAR IA Report shall, in particular, contain general and aggregated information on the Limited Exclusivity Agreements, Restricted Use Agreements or IP Applications that were concluded/ made by the Consortium and the Centers, subject to any confidentiality obligations of the Consortium and/or the Centers 17.

  • As a general principle, such IP Applications shall not be made unless they are necessary for the further improvement of such Intellectual Assets or to enhance the scale or scope of impact on target beneficiaries, in furtherance of the CGIAR Vision.6.4.3 All IP Rights shall be exercised consistently with Articles 6.1 to 6.3 above.

  • As a general principle, such IP Applications shall not be made unless they are necessary for the further improvement of such Intellectual Assets or to enhance the scale or scope of impact on target beneficiaries, in furtherance of the CGIAR Vision.”The Consortium itself did not file any IP Applications, either patents or PVP, nor did it register any trademarks, in 2013.

  • The following table presents the indicative total budget of each IP and the minimum contribution to apply as associated member for each IP: Applications to several Innovation Programmes are subject to the attainment by the candidate of the minimum contribution for each Innovation Programme applied for.

  • Filings of IP Applications in foreign countries: Within six months of filing the Complete IP Application in India, IITI shall, based on available information, decide on the suitability of protection of the invention in foreign countries.

  • Filings of IP Applications in foreign countries: Within a reasonable period of filing the complete IP application in India, IIT GOA shall, based on available information decide on the suitability of protection of the invention in foreign countries.

  • Our products satisfy needs within the areas of energy savings, food preservati- 1 The actual figure is impossible to assess, since most products are customized, making an almost infinite number of pro- duct varieties possible.

  • Examples showing why Limited Exclusive Agreements or IP Applications are sometimes needed:Seasoned scientists that work in crop breeding have observed that if Centers continue to release materials with no protection (e.g. "freely available" as often stated in donor publications) extolling the work of Centers, exactly the opposite happens.

  • As a general principle, such IP Applications shall not be made unless they are necessary for the further improvementof such Intellectual Assets or to enhance the scale or scope of impact on target beneficiaries, in furtherance of the CGIARVision.” In order to better assess compliancewith Article 6.4.2, the FC IP Group addressed follow-up questions through the Consortium Office to the Center for 5 of the 6 provisional patent applications.

Related to IP Applications

  • Applications means all of the following: “New Drug Application” (“NDA”), “Abbreviated New Drug Application” (“ANDA”), “Supplemental New Drug Application” (“SNDA”), or “Marketing Authorization Application” (“MAA”), the applications for a Product filed or to be filed with the FDA pursuant to 21 C.F.R. Part 314 et seq., and all supplements, amendments, and revisions thereto, any preparatory work, registration dossier, drafts and data necessary for the preparation thereof, and all correspondence between the Respondent and the FDA related thereto. The term “Application” also includes an “Investigational New Drug Application” (“IND”) filed or to be filed with the FDA pursuant to 21 C.F.R. Part 312, and all supplements, amendments, and revisions thereto, any preparatory work, registration dossier, drafts and data necessary for the preparation thereof, and all correspondence between the Respondent and the FDA related thereto.

  • Third Party Applications means online, Web-based applications and offline software products that are provided by third parties and are identified as third-party applications, including but not limited to those listed on the AppExchange and the Reseller Application.

  • Access Application means an application for Access Rights as described in section 3.7;

  • Uniform application means the current version of the national association of insurance commissioners uniform application for resident and nonresident insurance producer licensing.

  • Mobile Application means a specialized software program downloaded onto a wireless communication device.

  • Patent means (a) all patents and patent applications in any country or supranational jurisdiction in the Territory, (b) any substitutions, divisionals, continuations, continuations-in-part, provisional applications, reissues, renewals, registrations, confirmations, re-examinations, extensions, supplementary protection certificates and the like of any such patents or patent applications, and (c) foreign counterparts of any of the foregoing.

  • Customer Application means a software program that Customer creates or hosts using the Services.

  • Patents means all patents, patent applications and like protections including without limitation improvements, divisions, continuations, renewals, reissues, extensions and continuations-in-part of the same.

  • Biologics License Application or “BLA” means an application requesting permission from the FDA to introduce, or deliver for introduction, a biological product into interstate commerce, or any similar application or submission for marketing authorization of a product filed with a Regulatory Authority to obtain Regulatory Approval for such product in a country or group of countries.

  • Complete application means a document prepared in

  • international application means an application filed under this Treaty;

  • Marketing Authorization Application or “MAA” means a Marketing Authorization Application, Biologics License Application or similar application, as applicable, and all amendments and supplements thereto, submitted to the FDA, or any equivalent filing in a country or regulatory jurisdiction other than the U.S. with the applicable Regulatory Authority, to obtain marketing approval for a pharmaceutical or diagnostic product, in a country or in a group of countries.