Generic Rules definition

Generic Rules means these Generic Rules for Interest Groups made in accordance with the Constitution and as amended from time to time;
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Generic Rules means the rules made, or amended, by the Society in general meeting from time to time, for the formation, operation, management and dissolution of specific groups or committees of the Society or different classes of Constituent Units;
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Examples of Generic Rules in a sentence

  • Alterations and additions to these Generic Rules may only be made by the Society in general meeting.

  • These Generic Rules are subject to the Constitution of The Australian Psychological Society Limited (the “Society”).

  • A copy of the Generic Rules for Colleges will be available through the Society’s website at all times.

  • Please also refer to Generic Playing Condition 4: with the exception of Generic Rules 4.3 and 4.6 as varied hereunder.

  • Rules Governing Candidature See Generic Rules for Undergraduate Awards in the Rules section of this Handbook, in conjunction with specific Rules and the Schedule of Units below.

  • A copy of the Generic Rules will be available through the Society’s website at all times.

  • These Generic Rules are subject to the Constitution of The Australian Psychological Society Limited (the "Society").

  • Applications will be assessed against the criteria for grades of membership of a College and successful applicants will be elected or admitted to membership of a College in accordance with the provisions of these Generic Rules and with any other written requirements as may be additionally provided in the Standing Orders.

  • A reading of the Generic Rules shows, in my opinion, that once the targets set are achieved the defendant would be contractually bound by its own rules to pay the bonus to persons, such as the plaintiff, who qualified in all respects, if it were not for the provisions of clause 11.

  • Information costs are a crucial factor because they minimize the advantage when searching for better offers.

Related to Generic Rules

  • Generic String means a string consisting of a word or term that denominates or describes a general class of goods, services, groups, organizations or things, as opposed to distinguishing a specific brand of goods, services, groups, organizations or things from those of others.

  • Organic rules means the public organic record and private organic rules of an entity.

  • Generic Drug means any Prescription Drug approved by the FDA that has the same bio-equivalency as a specific Brand Name Drug.

  • Generic Version means, with respect to a Licensed Product, a product (including a “biogeneric,” “follow-on biologic,” “follow-on biological medicine or product,” “follow-on protein product,” “similar biological medicine or product,” or “biosimilar product”) that: (a) within the U.S., is “biosimilar” or “interchangeable,” with respect to such Licensed Product as evaluated by the FDA or otherwise determined by Applicable Law; or (b) in the ROW, is determined by the applicable Regulatory Authority or by Applicable Law to be “similar,” “comparable,” “interchangeable,” “bioequivalent,” or “biosimilar” to such Licensed Product. For clarity, a Biosimilar of a Licensed Product shall constitute a Generic Version of such Licensed Product.

  • Diagnostic clinical procedures manual means a collection of written procedures that describes each method (and other instructions and precautions) by which the licensee performs diagnostic clinical procedures; where each diagnostic clinical procedure has been approved by the authorized user and includes the radiopharmaceutical, dosage, and route of administration.

  • Generic name means a short title which is descriptive of the premium and benefit patterns of a policy or a rider.

  • regulated product means a consumer product for which a VOC standard is specified in section 94509(a), and

  • 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.

  • HIPAA Rules means the Privacy, Security, Breach Notification, and Enforcement Rules at 45 CFR Part 160 and Part 164.

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

  • HKIAC Rules shall have the meaning ascribed to it in Section 10.13(a).

  • Collaborative pharmacy practice agreement means a written and signed

  • Positive Behavioral Theory and Practice means a proactive approach to individual behavior and behavior interventions that:

  • Regulatory Disruption Any event that Dealer, based on the advice of counsel, determines makes it reasonably necessary or appropriate with regard to any legal, regulatory or self-regulatory requirements or related policies and procedures that generally apply to transactions of a nature and kind similar to the Transaction and have been adopted in good faith by Dealer for Dealer to refrain from or decrease any market activity in connection with the Transaction. Settlement:

  • FCA Rules means the Rules included within the FCA Handbook issued by the FCA.

  • M&A Rules means the Provisions on Merging and Acquiring Domestic Enterprises by Foreign Investors, which was promulgated by six Governmental Agencies, namely, the Ministry of Commerce, the State-owned Assets Supervision and Administration Commission, the State Administration for Taxation, the State Administration for Industry and Commerce, the China Securities Regulatory Commission (the “CSRC”), and the State Administration of Foreign Exchange, on August 8, 2006 and became effective on September 8, 2006, as amended by the Ministry of Commerce on June 22, 2009.

  • Applicable Rules means Section 10D of the Exchange Act, Rule 10D-1 promulgated thereunder, the listing rules of the national securities exchange or association on which the Company’s securities are listed, and any applicable rules, standards or other guidance adopted by the Securities and Exchange Commission or any national securities exchange or association on which the Company’s securities are listed.

  • 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.

  • Business Rules means the business rules established by JSCC regarding its Financial Instruments Obligation Assumption Service for CDS Transactions, as amended, if applicable.

  • Country Risks means with respect to any Foreign Depository: (a) the financial infrastructure of the country in which it is organized, (b) such country’s prevailing custody and settlement practices, (c) nationalization, expropriation or other governmental actions, (d) such country’s regulation of the banking or securities industry, (e) currency controls, restrictions, devaluations or fluctuations, and (f) market conditions which affect the order execution of securities transactions or affect the value of securities.

  • Regulatory Body means those government departments and regulatory, statutory and other entities, committees, ombudsmen and bodies which, whether under statute, rules, regulations, codes of practice or otherwise, are entitled to regulate or investigate the matters dealt with in this Agreement or any other affairs of the Provider or the Department, including, without limitation Ofsted, the European Commission and the European Court of Auditors;

  • 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

  • Automated drug dispensing system means a mechanical or electronic system that performs

  • Regulatory Authority means, with respect to any national, supra-national, regional, state or local regulatory jurisdiction, any agency, department, bureau, commission, council or other governmental entity involved in the granting of a Regulatory Approval for such jurisdiction.

  • ACH Rules means the NACHA Operating Rules and NACHA Operating Guidelines, as in effect from time to time.

  • Designated country end product means a WTO GPA country end product, a Free Trade Agreement country end product, a least developed country end product, or a Caribbean Basin country end product.