Standing Application definition

Standing Application means an application for the issue of Units on a regular and periodic basis;
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Standing Application means an application, whether or not in writing, by or on behalf of a Unit Holder or applicant for Units that is intended to have continuing force in respect of all moneys from whatever source made available to the Trustee for the time being by or on account of that Unit Holder or applicant including funds made available under a facility for crediting a bank account in the name of the Trustee;
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Examples of Standing Application in a sentence

  • Thermal limiter tripped• Call authorized service person for replacement.Dryer doesn’t heatFuse is blown/circuit breaker• Check the house fuse/circuit breaker box and replace is tripped, the dryer mayboth fuses or reset both breakers.

  • Course preferences Major Location Duration Commencement date ADVANCED STANDING Are you seeking advanced standing for previous study?Yes NoIf ‘Yes’ complete an Advanced Standing Application Form (www.scu.edu.au/advancedstanding), with supporting documentation including a certified copy of the transcript, comprehensive syllabus details for each relevant unit (descriptions, learning hours, assessment methods and explanation of weighting of each unit).

  • PROGRAM OF STUDYCourse preferences Major Location Duration Start date ADVANCED STANDING Are you seeking advanced standing for previous study?Yes NoIf ‘Yes’ complete an Advanced Standing Application Form (scu.edu.au/advancedstanding), with supporting documentation including a certified copy of the transcript, comprehensive syllabus details for each relevant unit (descriptions, learning hours, assessment methods and explanation of weighting of each unit).

  • Every student seeking readmission will be evaluated on an individual basis after having completed the Advanced Standing Application available in the Nursing Program office or from the Nursing Program website.

  • In such event:a unless the Manager determines otherwise, each Standing Application will be deemed to be cancelled; andb the Manager will not after the date specified in the notice issue any further Units under this Deed or in respect of such Fund or Funds for the specified period or until the relevant Fund(s) are terminated, whichever situation applies.

  • In fact, there is no evidence that these organizations are even aware of the new class definition proposed for the first time during the hearing of the Standing Application.

  • The Manager may, in its absolute discretion, accept or reject in whole or in part any application for Units in a Fund (including one made by virtue of a Standing Application), and the Manager is not required to give any reason for any such rejection.

  • An application may be designated as a Standing Application for an amount per month (or such other period as the Manager shall determine) at least equal to any applicable Unit Minimum, and may include an authorisation to the Manager to initiate direct debits to a bank account nominated by the applicant for relevant application amounts to be credited to the Supervisor.

  • Transfer students and others with special circumstances necessitating exceptions to these requirements must request special acceptance in writing to the Music Education Area Chairperson.Professional Standing Application Review and DecisionsThe transcript, e-portfolio and practica audits required forapplications must be completed after students’ completed course grades are available and deadlines for practicum paperwork submission have passed.

  • Standing Application Forms, when completed should be forwarded to the Supervisor who will forward the original copy to Human Resources and a receipt copy to the applicant.

Related to Standing Application

  • Planning Application means the application for [outline/full] planning permission dated [ ] bearing the Council’s reference number [ ];

  • Patent Application means an application for patent protection for a CRADA Subject Invention with the United States Patent and Trademark Office (“U.S.P.T.O.”) or the corresponding patent-issuing authority of another nation.

  • Regulatory Approval Application means an application to seek regular or expedited Regulatory Approval of the Licensed Product for sale or marketing in any country(ies) or Region(s) in the Territory, as defined in the applicable Laws and filed with the Regulatory Authority of such country(ies) or Region(s).

  • Licensed Application means an Application that (a) meets and complies with all of the Documentation and Program Requirements, and (b) has been selected and digitally signed by Apple for distribution, and includes any additional permitted functionality, content or services provided by You from within an Application using the In-App Purchase API.

  • Marketing Approval Application or “MAA” means a New Drug Application (or its equivalent), as defined in the U.S. Food, Drug and Cosmetic Act and the regulations promulgated thereunder, or any corresponding or similar application, registration or certification in any country.

  • Account Application or “Application” shall mean the application, as may be amended from time to time, by which this Agreement is established between the Depositor (or following the death of the Depositor, the Beneficiary) and the Custodian. The statements contained therein shall be incorporated into this Agreement.

  • SAP Application(s) means all Packages (i.e. all Software and Third Party Software) licensed under the Agreement and/or SAP cloud services for which Customer has a valid subscription, excluding User Interfaces for ERP, SAP Technology Solutions and all database Packages.

  • Patent Applications means all published and unpublished nonprovisional and provisional patent applications, reexamination proceedings, invention disclosures and records of invention, applications for certificates of invention and priority rights, in any country and regardless of formal name, including without limitation, substitutions, continuations, continuations-in-part, divisions, renewals, revivals, reissues, re-examinations and extensions thereof.

  • Marketing Authorization Application or “MAA” means an application to the appropriate Regulatory Authority for approval to sell the Product (but excluding Pricing Approval) in any particular country or regulatory jurisdiction.

  • Approval Application means a BLA, NDA or similar application or submission for a Product filed with a Regulatory Authority in a country or group of countries to obtain marketing approval for a biological or pharmaceutical product in that country or group of countries.

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

  • Initial application means the Application first provided to MFA on or before an Application Deadline to request an allocation of Tax Credits.

  • Commercial applicator means any person, unless exempted in I(4) hereunder, whether or not the person is a private applicator with respect to some uses, who:

  • Drug Application means a new drug application, an abbreviated drug application, or a product license application for any Product, as appropriate, as those terms are defined in the FDCA.

  • Development Application means the development application identified in Item 5 of Schedule 1 and includes all plans, reports models, photomontages, material boards (as amended supplemented) submitted to the consent authority before the determination of that Development Application.

  • international application means an application filed under this Treaty;

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

  • Patent Cooperation Treaty means the Patent Cooperation Treaty done at Washington on June 19, 1970;

  • 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.

  • 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.

  • Drug Approval Application means, with respect to a Licensed Product in the Territory, an application for Regulatory Approval for such product in a country in the Territory. For purposes of clarity, Drug Approval Application shall include, without limitation, (a) an NDA or BLA (for U.S.) or MAA (for Europe); (b) a counterpart of an NDA, BLA or MAA in any country or region in the Territory; and (c) all supplements (including supplemental applications such as sNDAs) and amendments to the foregoing.

  • New Drug Application means a New Drug Application filed with the FDA in accordance with Applicable Law.

  • Regulatory Approval means, with respect to a Product in any country or jurisdiction, any approval (including where required, pricing and reimbursement approvals), registration, license or authorization from a Regulatory Authority in a country or other jurisdiction that is necessary to market and sell such Product in such country or jurisdiction.

  • Project Application means the federal Section 5311 operating assistance project application submitted by the Municipal Corporation to, and as approved by the Commissioner for the Project described in Appendix C of this Agreement, including all project supporting information submitted therewith.

  • Client Application means an application developed by Customer that a) utilizes the Runtime Product, b) is installed fully on an end user’s machine, with all report processing local to that machine, and c) adds significant and primary functionality to the Runtime Product.

  • Pricing Approval means such mandatory governmental approval, agreement, determination or decision establishing prices for the Product that can be charged and/or reimbursed in regulatory jurisdictions where the applicable Governmental Authorities approve or determine the price and/or reimbursement of pharmaceutical products.