Or equal approved definition

Or equal approved means that products other than those specified may be used provided that the contractor satisfies the Architect/Contract Administrator as to their suitability and obtains his/her written approval. The Architect/Contract Administrator reserves the right to insist on the specified product if such approval is not given.
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Or equal approved means that products other than those specified may be used provided that the contractor satisfies the Project Manager as to their suitability and obtains his written approval. The Project Manager reserves the right to insist on the specified product if such approval is not given.
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Or equal approved means that products other than those specified may be used provided that the Tenderer satisfies the Architect/Clients representative as to their suitability and obtains his written approval. The Architect/Clients representative reserves the right to insist on the specified product if such approval is not given.
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Examples of Or equal approved in a sentence

  • Or equal approved by the Project Manager and Department in accordance with General Conditions.

  • Or equal approved by the Project Manager in accordance with General Conditions.

  • As agency guidance explains, where a laboratory bills Medicare under an NPI associated with the laboratory and other operating units (such as a physician’s office or other parts of a hospital), then the majority-of-revenues calculation includes revenues of all units reporting under that NPI, regardless whether they provide laboratory services.26 These extra, non-laboratory revenues diminish the significance of CLFS and PFS laboratory revenues relative to the entity’s entire Medicare revenues.

  • Or equal, approved in accordance with Division 01, General Requirements, for substitutions.

  • Ceiling to be manufactured and supplied by: OWA (UK) Ltd Unit 10 Perth Trading Estate Perth Avenue Slough SL1 4XX Tel – 01753 552 489 Or equal approved.

  • Manufacturers/Types: Westing house Type NQO" General Electric 'Type NLAB" Square D 'Type NQO" I.T.E. 'Type NPAB" Or equal approved by the Engineer.

  • Or equal, approved in accordance with Special Conditions requirements for substitutions.

  • QUESTION: Section 15059 1.4.D.3. - Sump Pump specs says "Or equal, approved in writing by Engineer and Owner prior to bid opening date." Is Barnes an acceptable manufacturer for the small sump pump in Shaft P?ANSWER: Subject to compliance with the Contract Documents, Barnes is an acceptable manufacturer for the small sump pump in Shaft P.

  • Or equal approved by the Project Manager and Department in accordance with General Conditions.2.06 Nails: (The use of staples to install shingles is PROHIBITED) Hot-dip galvanized 11 or 12-gage, sharp pointed, conventional roofing nails with barbed shanks, minimum 3/8" diameter head and of sufficient length to penetrate through sheathing.

  • Commercial Door and Hardware, Inc.B. Or equal approved by ArchitectC.

Related to Or equal approved

  • medically approved means certified by a medical practitioner;

  • CAISO-Approved Meter means any revenue quality, electric energy measurement meter furnished by Seller, that (a) is designed, manufactured and installed in accordance with the CAISO’s metering requirements, or, to the extent that the CAISO’s metering requirements do not apply, Prudent Electrical Practices, and (b) includes all of the associated metering transformers and related appurtenances that are required in order to measure the net electric energy output from the Generating Facility.

  • Roll-on product means any antiperspirant or deodorant that dispenses active ingredients by rolling a wetted ball or wetted cylinder on the affected area.

  • MAA Approval means approval by the EMEA of a marketing authorization application (“MAA”) filed with the EMEA for the applicable Licensed Product under the centralized European procedure. If the centralized EMEA filing procedure is not used, MAA Approval shall be achieved upon the first Approval for the applicable Licensed Product in any two of the following countries: France, Germany, Italy, Spain or the United Kingdom.

  • Certified Remanufacture System or Verified Engine Upgrade means engine upgrades certified or verified by EPA or CARB to achieve a reduction in emissions.

  • 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.

  • Semi-annual (2/Year) sampling frequency means the sampling shall be done during the months of June and December, unless specifically identified otherwise.

  • Good Laboratory Practices or “GLP” means the then-current good laboratory practice standards promulgated or endorsed by the FDA, as defined in U.S. 21 C.F.R. Part 58 (or such other comparable regulatory standards in jurisdictions outside the United States, as they may be updated from time to time).

  • Good Laboratory Practice or “GLP” means the applicable then-current standards for laboratory activities for pharmaceuticals (including biologicals) or vaccines, as applicable, as set forth in the Act and any regulations or guidance documents promulgated thereunder, as amended from time to time, together with any similar standards of good laboratory practice as are required by any Regulatory Authority having jurisdiction over the applicable activity.

  • Collaborative pharmacy practice means a practice of pharmacy whereby one or

  • Major Market Countries means the United States, Japan, England, Germany, France, Italy and Spain.

  • Approved Market means the Over-the-Counter Bulletin Board, the Nasdaq Stock Market, the New York Stock Exchange or the American Stock Exchange.

  • Peer-reviewed medical literature means a published scientific study in a journal or other publication in which original manuscripts have been published only after having been critically reviewed for scientific accuracy, validity and reliability by unbiased independent experts, and that has been determined by the international committee of medical journal editors to have met the uniform requirements for manuscripts submitted to biomedical journals. Peer-reviewed medical literature does not include publications or supplements to publications that are sponsored to a significant extent by a pharmaceutical manufacturing company or health carrier.

  • Semi-annual (2/Year) sampling frequency means the sampling shall be done during the months of June and December, unless specifically identified otherwise.

  • Government Apprenticeship Programme “ means training which is funded by the Government via the National Apprenticeship Service.

  • Number of Students Who Began the Program means the number of students who began a program who were scheduled to complete the program within 100% of the published program length within the reporting calendar year and excludes all students who cancelled during the cancellation period.

  • Developmentally appropriate means suitable to the chronological age range and developmental characteristics of a specific group of children.

  • 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.

  • Initial approval means authorization to admit students and enter into contractual agreements for clinical facilities. It is granted only after an application has been submitted, reviewed and a survey visit made by the Board. No students shall be admitted to the program until the institution has received written notification that initial approval has been granted. Failure to comply will delay initial approval.

  • Number of Students Who Began Program means the number of students who began the program who are scheduled to complete the program within the reporting calendar year.

  • Final Approval means the Court’s order granting final approval of the Settlement.

  • TARGET System means the Trans-European Automated Real-Time Gross Settlement Express Transfer (known as TARGET2) System which was launched on 19 November 2007 or any successor thereto.

  • 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.

  • Phase 3 Clinical Trial means a pivotal clinical trial in humans performed to gain evidence with statistical significance of the efficacy of a product in a target population, and to obtain expanded evidence of safety for such product that is needed to evaluate the overall benefit-risk relationship of such product, to form the basis for approval of an NDA and to provide an adequate basis for physician labeling, as described in 21 C.F.R. § 312.21(c) or the corresponding regulation in jurisdictions other than the United States.

  • Phase 2 Clinical Trial means a human clinical trial of a product in any country that would satisfy the requirements of 21 C.F.R. 312.21(b) and is intended to explore a variety of doses, dose response, and duration of effect, and to generate initial evidence of clinical safety and activity in a target patient population, or a similar clinical study prescribed by the relevant Regulatory Authorities in a country other than the United States.

  • Relevant Electric Retail Regulatory Authority means an entity that has jurisdiction over and establishes prices and policies for competition for providers of retail electric service to end- customers, such as the city council for a municipal utility, the governing board of a cooperative utility, the state public utility commission or any other such entity.