Specialty Product definition

Specialty Product means chemicals and materials which are not Commodity Products.
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Specialty Product means those products/items enumerated in Attachment C.
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Specialty Product means any current or potential new product, platform, service or account that would reasonably be expected to require enhanced reporting, monitoring and oversight to ensure compliance with the Bank Secrecy Act and state and federal anti-money laundering Laws.
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Examples of Specialty Product in a sentence

  • The aforementioned list is illustrative only (not exhaustive) and may include other supplies, equipment, and services based on the patient’s needs, prescriber instructions, payer requirements, and/or the Specialty Product manufacturer’s requirements.

  • ESI Specialty Pharmacy is the exclusive provider of Specialty Products for the reimbursement rates shown on the Exclusive ESI Specialty Pharmacy Specialty Product List.

  • Any Specialty Product dispensed at a Participating Pharmacy (for example, limited distribution products not then available through ESI Specialty Pharmacy or overrides) will be reimbursed at the standard Participating Pharmacy Specialty Product rates shown below.

  • Any Specialty Product dispensed from a pharmacy other than CuraScript (for example, limited distribution products not then available through CuraScript or overrides) will be reimbursed at ESI’s standard “open” network Specialty Product rates shown below.

  • At the date of Licensee’s notice to Teva of its election to treat such Distribution Product as a Specialty Product, such product shall be treated, for all intents and purposes under this Agreement, as a Specialty Product and all provisions and undertakings of Licensee relating to a Specialty Product under this Agreement shall apply to such product.

  • Licensee shall provide Teva with drafts of Regulatory Materials in original language English for the Specialty Product to be submitted by or on behalf of Licensee or its Affiliates in the Territory, excluding any portions of such Regulatory Materials provided by Teva to Licensee, sufficiently in advance of submission to allow for Teva’s review and comment.

  • If Client elects Exclusive Specialty, then ESI Specialty Pharmacy is the exclusive provider of Specialty Products for the reimbursement rates shown on the Exclusive ESI Specialty Pharmacy Specialty Product List.

  • Licensee will be responsible, with the assistance and cooperation of Teva or its Affiliates as provided in this Article 4, for Development to obtain or maintain Regulatory Approval in the Territory for the Specialty Product.

  • CuraScript is the exclusive provider of Specialty Products for the reimbursement rates shown on the Exclusive CuraScript Specialty Product List.

  • At each regularly scheduled JDC meeting, each Party shall provide the other Party with a list and schedule of any in-person meeting or teleconference with Regulatory Authorities (or related advisory committees) in the Territory planned for the next calendar quarter that relates to the Specialty Product in the Field.


More Definitions of Specialty Product

Specialty Product the pharmaceutical product set forth on Exhibit B, in the forms, presentations, formulations, methods of administration and dosage forms set forth and amended from time to time therein.
Sample 1
Specialty Product means those injectable and non-injectable drugs typically having one or more of several key characteristics and may include generic equivalents and biosimilar products: frequent dosing adjustments and intensive clinical monitoring to decrease the potential for drug toxicity and increase the probability for beneficial treatment outcomes; intensive patient training and compliance assistance to facilitate therapeutic goals; limited or exclusive product availability and distribution; specialized product handling and/or administration requirements and/or cost in excess of $500 for a 30-day supply. SCL will maintain a Specialty Product list that contains Specialty Products that are eligible for specialty Guaranteed Rebates. “Third Party Administrator (TPA) means any individual or firm appointed by Sponsor to perform certain administrative services pursuant to a contract or agreement between Sponsor and TPA. “Usual & Customary” (U&C) is the lowest price a pharmacy would charge if the customer were paying cash, including senior citizen discounts and frequent shopper discounts.
Sample 1
Specialty Product means a Branded Rx Product designated as specialty product by a majority of third party industry sources, including but not limited to, CMS, health insurance providers, and pharmacy benefit managers, or Merchandise that meets specific criteria (collectively, the “Criteria”), including but not limited to the following:
Sample 1
Specialty Product shall have the meaning set forth in Recital A.
Sample 1
Specialty Product means those injectable and non-injectable drugs on the Specialty Product List, which must have a cost exceeding $600 per thirty day's supply and have one or more of the following key characteristics: frequent dosing adjustments and intensive clinical monitoring to decrease the potential for drug toxicity and increase the probability for beneficial treatment outcomes; intensive patient training and compliance assistance to facilitate therapeutic goals; limited or exclusive product availability and distribution; and/or specialized product handling and/or administrationrequirements.
Sample 1

Related to Specialty Product

  • Third Party Products means the Third Party Software and Third Party Hardware.

  • Product means any deliverable under the Contract, which may include commodities, services, technology or software.

  • 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.

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

  • 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.

  • Third Party Product means a product (whether hardware, software or services) supplied to you by a third party;

  • Licensed Product means any method, process, composition, product, service, or component part thereof that would, but for the granting of the rights set forth in this Agreement, infringe a Valid Claim contained in the Licensed Patents.

  • WTO GPA country end product means an article that—

  • Special food product means a food product that is all of the following:

  • Hemp products means all products made from industrial hemp,

  • Aerosol coating product means a pressurized coating product containing pigments or resins that dispenses product ingredients by means of a propellant, and is packaged in a disposable can for hand-held application, or for use in specialized equipment for ground traffic/marking applications.

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

  • Competing Products means any product or service in existence or under development that competes with any product or service of the Company Group about which the Participant obtained Confidential Information or for which the Participant provided advisory services or had sales, origination, marketing, production, distribution, research or development responsibilities in the last twenty-four (24) months of employment with the Company Group.

  • Marihuana-infused product means a topical formulation, tincture, beverage, edible substance, or similar product containing marihuana and other ingredients and that is intended for human consumption.

  • Medical marijuana product means a product that contains cannabinoids that have been extracted from plant material or the resin therefrom by physical or chemical means and is intended for administration to a licensed patient, including but not limited to concentrates, oils, tinctures, edibles, pills, topical forms, gels, creams, and other derivative forms, except that this term does not include live plant forms.

  • Cannabis products means cannabis that has undergone a process whereby the plant material has been transformed into a concentrate, including, but not limited to, concentrated cannabis, or an edible or topical product containing cannabis or concentrated cannabis and other ingredients.

  • New Products means any product which is not an Enhanced Product or 2 Existing Product but which is substantially similar to an Existing Product with respect to design and function and possesses reasonable performance improvements. If Company desires to purchase an Enhanced or New Product(s) from Supplier, Company shall so notify Supplier and provide Supplier the opportunity to manufacture such Enhanced or New Product(s), subject to the following conditions and procedures.

  • Marijuana products means concentrated marijuana products and marijuana products that are comprised of marijuana and other ingredients and are intended for use or consumption, such as, but not limited to, edible products, ointments, and tinctures.

  • Generic Product means a product which (a) contains as its active pharmaceutical ingredient a compound that is (or is substantially the same as) the Licensed Compound or the active pharmaceutical contained in a Unity Bcl-2 [***] Product, and (b) has been placed on the market pursuant to a validly granted marketing authorization.

  • Specialty drug means a prescription drug that:

  • Commercial Product means any such product as defined in FAR 2.101.

  • Aerosol product means a pressurized spray system that dispenses product ingredients by means of a propellant contained in a product or a product's container, or by means of a mechanically induced force. “Aerosol Product” does not include “Pump Spray.”

  • Specialty Drugs means drugs listed on the Approved Drug List meeting certain criteria, such as:

  • Biological product means a virus, therapeutic serum, toxin, antitoxin, vaccine, blood, blood component or derivative, allergenic product, protein other than a chemically synthesized polypeptide, or analogous product, or arsphenamine or any derivative of arsphenamine or any other trivalent organic arsenic compound, applicable to the prevention, treatment, or cure of a disease or condition of human beings.

  • End Products as used in this clause, means those articles, materials, and supplies to be acquired for public use under this contract.

  • complex product means a product which is composed of multiple components which can be replaced permitting disassembly and re-assembly of the product.