Prototype SFE definition

Prototype SFE means the Prototype Agreements Scheme Statement of Financial Entitlements(d);
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Examples of Prototype SFE in a sentence

  • For the purposes of this paragraph, “Blend A prototype agreement” and “Blend B prototype agreement” have the same meaning as in the Prototype SFE.

  • In Section 18 (Negotiated Annual Prototype Value) of the Prototype SFE, in sub-paragraph 18.8(b) (dealing with under-delivery of units of dental activity in previous financial year or in the current financial year), for “that was agreed would be carried forward” substitute “that was agreed between the Board and the contractor would be carried forward”.

  • The standards issued in the development of this law will only have a tax effect when the tax laws specifically refer to them or when said laws do not regulate the subject.” This enables us to confirm the separation between the accounting information and the tax system.

  • Further in the calculations we will use data from Table 2, as well as the data derived therefrom.To give the exact definition of risk extent is an impossible task.

Related to Prototype SFE

  • Prototype means a first model or design that has not been produced in batches, and from which the finished cosmetic product is copied or finally developed.

  • Prototype Sponsor Means the entity specified on the Adoption Agreement which sponsors this prototype plan.

  • Submitter means any person or en- tity who provides confidential commer- cial information to the government. The term ‘‘submitter’’ includes, but is not limited to, corporations, state gov- ernments, and foreign governments.

  • Brand Name Specification means a specification limited to one or more items by manufacturers’ names or catalogue number.

  • Brand Name or Equal Specification means a specification which uses one or more manufacturer’s names or catalogue numbers to describe the standard of quality, performance, and other characteristics needed to meet District requirements, and which provides for the submission of equivalent products.

  • layout plan means a plan of the project depicting the division or proposed division of land into plots, roads, open spaces, amenities, etc. and other details as may be necessary;

  • Commercial Software means Software developed or regularly used that: (i) has been sold, leased, or licensed to the general public; (ii) has been offered for sale, lease, or license to the general public; (iii) has not been offered, sold, leased, or licensed to the public but will be available for commercial sale, lease, or license in time to satisfy the delivery requirements of this Contract; or (iv) satisfies a criterion expressed in (i), (ii), or (iii) above and would require only minor modifications to meet the requirements of this Contract.

  • Participating Prescription Drug Provider means an independent retail Pharmacy, chain of retail Pharmacies, mail-order Pharmacy or specialty drug Pharmacy which has entered into an agreement to provide pharmaceutical services to participants in the benefit program. A retail Participating Pharmacy may or may not be a select Participating Pharmacy as that term is used in the Vaccinations Obtained Through Participating Pharmacies section.

  • Contract Specifications means the principal trading terms in CFD (for example Spread, Swaps, Lot Size, Initial Margin, Necessary Margin, Hedged Margin, the minimum level for placing Stop Loss, Take Profit and Limit Orders, financing charges, charges etc) for each type of CFD as determined by the Company from time to time.

  • Fabrication means making up data or results and recording or reporting them.

  • Authorized nuclear pharmacist means a pharmacist who:

  • Participating Clinical Laboratory means a Clinical Laboratory which has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • Application Review Start Date means the later date of either the date on which the District issues its written notice that the Applicant has submitted a completed Application or the date on which the Comptroller issues its written notice that the Applicant has submitted a completed Application and as further identified in Section 2.3.A of this Agreement.

  • Participating manufacturer means that term as defined in the master settlement agreement.

  • Basic Comprehensive User Guide means the Ministry document titled Basic Comprehensive Certificates of Approval (Air) User Guide” dated April 2004 as amended.

  • District specification means the specifications followed by the State Govt. in the area where the work is to be executed.

  • technical specification means a document that prescribes technical requirements to be fulfilled by a product, process or service;

  • service delivery and budget implementation plan means a detailed plan approved by the executive mayor of a municipality in terms of section 53(l)(c)(ii) of the MFMA for implementing the municipality's delivery of municipal services and its annual budget, and which must indicate

  • Procurement Plan means the Recipient’s procurement plan for the Project, dated April 2, 2010, and referred to in paragraph 1.16 of the Procurement Guidelines and paragraph 1.24 of the Consultant Guidelines, as the same shall be updated from time to time in accordance with the provisions of said paragraphs.

  • Authorized aftermarket manufacturer means an organization that fabricates a part under a contract with, or with the express written authority of, the original component manufacturer based on the original component manufacturer’s designs, formulas and/or specifications.

  • State implementation plan or “SIP” means the plan adopted by the state of Iowa and approved by the Administrator which provides for implementation, maintenance, and enforcement of such primary and secondary ambient air quality standards as they are adopted by the Administrator, pursuant to the Act.

  • Prescription drug means any drug required by federal law or regulation to be dispensed only

  • Product Specification means a product specification for a Medical Device set out in Schedule 2;

  • Project Implementation Manual or “PIM” means the manual setting out the measures required for the implementation of the Project, as the same may be amended from time to time, subject to prior approval of the Association;

  • compatibility means compatibility as defined in point (10) of Article 2 of Directive (EU) 2019/770;

  • The Specification means the Specification annexed to or issued with G.T.C.C. and shall include the schedules & drawings attached thereto as well as all samples and pattern, if any.