NDCA definition

NDCA means the National Disciplinary Committee of Appeal; “NEC” means the National Executive Committee of the ANC; “NGC” means the National General Council of the ANC;
NDCA or the "Company"), and Xxxxx X. Xxxxxxxxx, an individual residing at 0000 Xxxxxxxx Xxxxx, Xxxxxxxxx, Xxxxx Xxxxxxxx 00000(xxx "Executive").
NDCA or the "Company"), and Ralph G. Dollander, an individual residing at 2601 Cloister Drive, Xxxxxxxxx, Xxxxx Xarolina 28211(the "Executive").

Examples of NDCA in a sentence

  • Electronic or printed versions or the webpage for a debate institute or the NDCA sponsored Open Evidence Project or similar sites.

  • Board Approval: The NDCA Board of Directors has final authority to approve grants and amounts.

  • Recognition • Grantees are required to acknowledge NDCA support by using the NDCA logo and credit-line on all promotional materials of the funded activity.

  • The North Dakota Council on the Arts (NDCA) is receiving ARP funds and they will need assistance in distributing those funds to the artists and organizations who need them.

  • In order to assist with this distribution, NDCA has asked the Minot Area Council of the Arts, as well as The Arts Partnership in Fargo, to pursue an LAA designation, which is necessary to distribute these federal funds.

  • The projects above create opportunities for capacity-building and implementation of data sharing across state agencies.

  • Overdue final reports will affect future eligibility to apply for and/or receive NDCA funding.

  • Play in each fixture shall commence at the time designated by the NDCA Inc.

  • For drug/alcohol testing, the employee will be reimbursed actual time worked with a minimum of five (5) hours call out at the overtime rate.

  • If they are not so operated the Umpires shall indicate accordingly in their report and a fine of $33 (incl $3 GST) for each offence shall be payable unless in the opinion of the NDCA Management Committee there are extenuating circumstances.


More Definitions of NDCA

NDCA means the National Disciplinary Commit tee of Appeal; "NCC" means the National Coordinating Commit tee of the BLF; "NGC" means National General Council
NDCA means the National Disciplinary Committee of Appeal;

Related to NDCA

  • NDC means National Drug Code.

  • Marketing Authorization Application or “MAA” means an application for Regulatory Approval in a country, territory or possession.

  • Tobacco products means cigars, cigarettes, cheroots, stogies, periques, granulated, plug cut, crimp cut, ready rubbed, and other smoking tobacco, snuff, snuff flour, moist snuff, cavendish, ping and twist tobacco, fine-cut and other chewing tobaccos, shorts, refuse scraps, clippings, cuttings and sweepings of tobacco, and other kinds and forms of tobacco, prepared in such manner as to be suitable for chewing or smoking in a pipe or otherwise, or both for chewing and smoking.

  • Tobacco product means any substance containing tobacco leaf, including but not limited to, cigarettes, cigars, pipe tobacco, hookah tobacco, snuff, chewing tobacco, dipping tobacco, bidis, blunts, clove cigarettes, or any other preparation of tobacco; and any product or formulation of matter containing biologically active amounts of nicotine that is manufactured, sold, offered for sale, or otherwise distributed with the expectation that the product or matter will be introduced into the human body by inhalation; but does not include any cessation product specifically approved by the U.S. Food and Drug Administration for use in treating nicotine or tobacco dependence.

  • Wholesale drug distributor means anyone engaged in the

  • Red Hat Products means Software, Services, Subscriptions and other Red Hat branded offerings made available by Red Hat.

  • Federal work authorization program means any of the electronic verification of work authorization programs operated by the United States Department of Homeland Security or any equivalent federal work authorization program operated by the United States Department of Homeland Security to verify information of newly hired employees, pursuant to the Immigration Reform and Control Act of 1986 (IRCA), D.L. 99-603.

  • Marketing Authorization means all approvals from the relevant Regulatory Authority necessary to market and sell a Product in any country (including without limitation, all applicable pricing and governmental reimbursement approvals even if not legally required to sell Product in a country).

  • ANDA means an Abbreviated New Drug Application filed with the FDA pursuant to its rules and regulations.

  • FDCA shall have the meaning ascribed to such term in Section 3.1(hh).

  • WTO GPA country end product means an article that—

  • Brand Name Drug means a Prescription Drug that has been given a name by a manufacturer or distributor to distinguish it as produced or sold by a specific manufacturer or distributor and may be used and protected by a trademark.

  • Tobacco product manufacturer means an entity that after the date of enactment of this Act directly (and not exclusively through any affiliate):

  • FFDCA means the United States Federal Food, Drug, and Cosmetic Act, 21 U.S.C. §301 et seq., as amended from time to time, together with any rules, regulations and requirements promulgated thereunder (including all additions, supplements, extensions, and modifications thereto).

  • low protein modified food product means a food product that is specially formulated to have less than one gram of protein per serving and is intended to be used under the direction of a Practitioner for the dietary treatment of an inherited metabolic disease, but does not include a natural food that is naturally low in protein; and

  • Anti-Static Product means a product that is labeled to eliminate, prevent, or inhibit the accumulation of static electricity. “Anti-Static Product” does not include “Electronic Cleaner,” “Floor Polish or Wax,” “Floor Coating,” and products that meet the definition of “Aerosol Coating Product” or “Architectural Coating.”

  • Commercial Supply Agreement has the meaning set forth in Section 6.1.

  • NDA means a New Drug Application, as defined in the regulations promulgated by the United States Food and Drug Administration, or any foreign equivalent thereof.

  • Drug Master File or “DMF” is described in 21 C.F.R. Part 314.420. A DMF is a submission to the FDA that may be used to provide confidential detailed information about facilities, processes, or articles used in the manufacturing, processing, packaging, and storing of one or more human drugs.

  • FD&C Act means the United States Federal Food, Drug, and Cosmetic Act (21 U.S.C. § 301 et seq.), as amended, and the rules and regulations promulgated thereunder.

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

  • Commercial sex act means any sex act on account of which anything of value is given to or received by any person.

  • Free Trade Agreement country end product means an article that—

  • Product brand name means the name of the product exactly as it appears on the principal display panel of the product.

  • FDA means the United States Food and Drug Administration and any successor agency thereto.

  • Free product means a contaminant that is present as a non-aqueous phase liquid for chemicals whose melting point is less than 30° C (e.g., liquid not dissolved in water).