Funding Approval Form definition

Funding Approval Form means the FHLB-PGH form that the Participating Member uses to request that approved Recoverable Assistance monies be placed in its demand deposit account at FHLB-PGH, as may be modified, amended, or supplemented by FHLB-PGH from time to time.
Funding Approval Form means the FHLB Dallas form that the Participating Member uses to request that approved Recoverable Assistance monies be placed in its demand deposit account at FHLB Dallas, as may be modified, amended, or supplemented by FHLB Dallas from time to time.
Funding Approval Form means the application requesting funding from MassCEC for the Internship Company’s selected intern(s) through the Program.

Examples of Funding Approval Form in a sentence

  • In order to access funds reserved for a Small Business Transaction, the Participating Member must submit a fully completed Funding Approval Form to FHLB-PGH at least two (2) Business Days prior to accessing such funds.The funds requested shall be deposited by FHLB-PGH into the Participating Member’s Demand Deposit Account at FHLB-PGH (the “ DDA”).

  • You should take your form to Medical Staffing ensuring;• Your form is fully completed and you have signed it• Obtain signature from Medical Staffing/Finance as appropriate• Collect the form / arrange for it to be sent back to you / arrange for it to be sent onwards as follows;o Foundation – LTFT Approval Form – Send to Foundation Schoolo GP & Specialty – Funding Approval Form – Send to HEKSS LTFT TeamPlease note it is your responsibility to track the form and follow it up with Medical Staffing/Finance.

  • In order to access funds reserved for a Small Business Transaction, the Participating Member must submit a fully completed Funding Approval Form to FHLB-PGH at least two (2) Business Days prior to accessing such funds.

  • The information in the closeout package will assist the Department in determining whether all requirements of the contract between the Department and the Grantee have been completed.The HUD 7082 Funding Approval Form The Grant Agreement between the Department of Housing and Urban Development (HUD) and the Grantee is made pursuant to the authority of Title I of the Housing and Community Development Act of 1974, as amended, (42 USC 5301 et seq.).

  • The submission of the HUD 7082 – Funding Approval Form is necessary as the form is the Grant Agreement between the Department of Housingand Urban Development (HUD) and the Grantee and is made pursuant to the authority of the HCDA, as amended, (42 USC 5301 et seq.).

  • Do not pay for a hotel with personal funds and expect reimbursement.Employee Travel Funding Approval Form Request for Materials (RFM) Hotel TaxExemption Form (without this an employee will be responsible for this cost out of pocket) GISD TravelExpense Summary Report (with hotel receipt) Note that even with this form, not all taxes will be exempted.

  • Execution of Funding Approval Form authorizes Skagit County to contract with McKinstry Essention, LLC in the amount of $115,966 for their professional services.8. Interlocal Agreement between North Sound Behavioral Health Organization, LLC and Skagit County for use of County-owned building located at 201 Lila Lane in Burlington.

  • The submission of the HUD 7082 – Funding Approval Form is necessary as the form is the Grant Agreement between the Department of Housing and Urban Development (HUD) and the Grantee and is made pursuant to the authority of the HCDA, as amended, (42 USC 5301 et seq.).

  • Taxes paid on food at restaurants are reimbursed, but gratuities are notreimbursed.Mileage & ParkingGISD employee,with possible GISD Fine Arts reimbursement (must be approved in advance).Employee Travel Funding Approval Form GISD TravelExpense Summary ReportMileage is only paid to the driver.

  • The next item for consideration was the authorization for execution of the Funding Approval, the Funding Approval Form and the Signatory Forms and Certification authorizing the Mayor, the City Manager, the Finance Director and the Chief Accountant to sign requisitions for CDBG funds in connection with the NC Department of Commerce Grant Agreement #04-E-1287.

Related to Funding Approval Form

  • Regulatory Approval Application means any application submitted to an appropriate Regulatory Authority seeking any Regulatory Approval.

  • 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.

  • Regulatory Approval means any and all approvals (including MAA Approval, and Pricing and Reimbursement Approval, if applicable), licenses, registrations, permits, notifications and authorizations (or waivers) of any Regulatory Authority that are necessary for the manufacture, use, storage, import, transport, promotion, marketing, distribution, offer for sale, sale or other commercialization of a Product in any country or jurisdiction.

  • NDA Approval means the Approval of an NDA by the FDA for a Product in the U.S.

  • FDA Approval means the approval, license, clearance or authorization of the FDA necessary for the marketing and sale of a product for human use in the United States.

  • MAA Approval means approval of an MAA by the applicable Regulatory Authority for marketing and sale of a Product in the Collaborator Territory, but excluding any Pricing and Reimbursement Approval.

  • Marketing Approval means all approvals, licenses, registrations or authorizations of the Regulatory Authority in a country, necessary for the manufacture, use, storage, import, marketing and sale of a Product in such country.

  • 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.

  • Pricing Approval means such governmental approval, agreement, determination or decision establishing prices for a Licensed 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.

  • Drug Approval Application means an application for Regulatory Approval required before commercial sale of a Product as a pharmaceutical product in a regulatory jurisdiction.

  • Required Regulatory Approvals means the Seller Required Regulatory Approvals and the Buyer Required Regulatory Approvals.

  • Master Account Approval List means the list of Attendee reservations and Dates which the Judicial Council has authorized the Contractor to xxxx associated sleeping room charges and tax against the Judicial Council’s Master Account.

  • Regulatory Approvals means any registrations, licenses, authorizations, permits or approvals issued by any Governmental Authority and applications or submissions related to any of the foregoing.

  • Marketing Authorization Application or “MAA” means an application for Regulatory Approval (but excluding Pricing Approval) in any particular jurisdiction other than the U.S.

  • Key Regulatory Approvals means those sanctions, rulings, consents, orders, exemptions, permits and other approvals (including the lapse, without objection, of a prescribed time under a statute or regulation that states that a transaction may be implemented if a prescribed time lapses following the giving of notice without an objection being made) of Governmental Entities as set out in Schedule C hereto;

  • Application Approval Date means the date that the Application is approved by the Board of Trustees of the District and as further identified in Section 2.3.B of this Agreement.

  • Requisite Regulatory Approvals has the meaning set forth in Section 7.01(b).

  • Product Approval means the approval of a Governmental Authority necessary for the marketing and sale of the Product in a given country or regulatory jurisdiction, which may include the approval of an MAA (but shall not include any Pricing Approvals).

  • Phase III Clinical Trials means a Clinical Trial for the Product on sufficient numbers of patients to generate safety and efficacy data to support Regulatory Approval in the proposed therapeutic indication, conducted in accordance with current good clinical practices and in accordance with a protocol that has been reviewed by the FDA and reflects any comments or concerns raised by the same.

  • IRB approval means the determination of the IRB that the research has been reviewed and may be conducted at an institution within the constraints set forth by the IRB and by other institutional and federal requirements.

  • Funding Authority means the body awarding the grant for the Project.

  • Phase II Clinical Trial means a controlled human clinical study that would satisfy the requirements of 21 CFR 312.21(b), conducted to study the effectiveness and establish the dose range of a Product for a particular Indication in patients with the disease or condition under study, including a Phase IIA Clinical Study or Phase IIB Clinical Study.

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

  • Account Opening Application Form means the application form/questionnaire completed by the Client, on-line on the Company’s Website and/or mobile application(s) and/or in hard copy, in order to apply for the Company’s Services under the Agreement and a Client Account, via which form/questionnaire the Company will obtain amongst other things information for the Client’s identification and due diligence, financial profile and appropriateness in accordance with the Applicable Regulations.

  • Approval of a vehicle means the approval of a vehicle type with regard to sound;

  • Phase III Clinical Trial means a human clinical trial of a product, the design of which is acknowledged by the FDA to be sufficient for such clinical trial to satisfy the requirements of 21 C.F.R. 312.21(c) (as amended or any replacement thereof), or a similar human clinical trial prescribed by the Regulatory Authority in a country other than the United States, the design of which is acknowledged by such Regulatory Authority to be sufficient for such clinical trial to satisfy the requirements of a pivotal efficacy and safety clinical trial.