EU Codes definition

EU Codes means EU Council Directive 2001/23/EC or any regulation, law or code enacted by any EU Member State to implement such directive.
EU Codes means the Balancing Code, the CAM Code and the Interoperability Code;

Examples of EU Codes in a sentence

  • Potential remedies included the creation of EU Codes of Conduct and certification of research activities, to increase harmonisation and confidence in compliance with the GDPR.

  • A specific implementation date is not proposed however this Modification needs to be implemented by 1st October 2015 to enable GB to be compliant with certain provisions of the EU Codes.

  • Secondly, as a separate GB Modification (outside of the EU Codes) a Workgroup has been established to investigate how the Storage technologies should be treated under the auspices of the GB Grid Code.

  • The TSO’s and NRA’s have agreed capacity bundling and matching rules between National Grid and its counterparties in line with the EU Codes which have now been finalised and are binding EU regulations.

  • As such it is a unique and unequaled collection of Dakota stories.When I learned more about our Dakota history and our stories, one of the first stories that I heard was that when we came to be as a people, we were placed at Bdote.

  • The only additional area that we could pursue is Interconnectors, however the EU Codes are focussed on Interconnection Points and therefore it would be inappropriate for us to pursue solutions in this area until we have assessed the impact of the new EU Codes.

  • The Workgroup considers that these arrangements are consistent with the ‘minimum change’ principle for EU changes impacting the UNC.In respect of the Moffat IP, the modification also clarifies how the requirements of EU Codes BAL, CAM and CMP will be given effect.

  • In particular, the CLASP model has provided the basis for the exploration of various potential savings scenarios for this report.EU Code of ConductThe EU Codes of Conduct (CoC) are voluntary initiatives involving for industry, experts and Member States.

  • The former is against the principle of neutrality spelled out in both the KPU and EU Codes of Conduct.

  • Therefore, the Supplier shall offer equipment with high energy efficiency, compliant with advanced international efficiency standards as e.g. the EU Codes of Conduct in their latest available version.


More Definitions of EU Codes

EU Codes the Balancing Code, the CAM Code and the Interoperability Code;

Related to EU Codes

  • Codes means the following including the latest amendments and/or replacements, if any:

  • GMP means the amount proposed by Contractor and accepted by Owner as the maximum cost to Owner for construction of the Project in accordance with this Agreement. The GMP includes Contractor’s Construction Phase Fee, the General Conditions Cost, the Cost of the Work, and Contractor’s Contingency amount.

  • JORC Code means the Australasian Code for Reporting of Exploration Results, Mineral Resources and Ore Reserves prepared by the Joint Ore Reserves Committee of the Australasian Institute of Mining and Metallurgy, Australian Institute of Geoscientists and Minerals Council of Australia, as amended;

  • Building Code Act means the Building Code Act, 1992, S.O. 1992, c.23, as amended;

  • Cathodic protection tester means a person who can demonstrate an understanding of the principles and measurements of all common types of cathodic protection systems as applied to buried or submerged metal piping and tank systems. At a minimum, such persons must have education and experience in soil resistivity, stray current, structure-to-soil potential, and component electrical isolation measurements of buried metal piping and tank systems.

  • StarCompliance Code of Ethics application means the web-based application used to electronically pre-clear personal securities transactions and file many of the reports required herein. The application can be accessed via the AB network at: https://alliance-ng.starcompliance.com/.

  • Clinical laboratory means a facility for the microbiological, serological, chemical, hematological, radiobioassay, cytological, immunohematological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of a disease or assessment of a medical condition.

  • Drug abuse means any pattern of pathological use of drugs that causes impairment in social or occupational functioning, or that produces physiological dependency evidenced by physical tolerance or by physical symptoms when it is withdrawn.

  • harmonised standard means harmonised standard as defined in point (c) of point 1 of Article 2 of Regulation (EU) No 1025/2012;

  • Licensed clinical social worker means an individual who meets the licensed clinical social worker requirements established in KRS 335.100.

  • 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.

  • EU means the European Union.

  • Loan Prod Code Rem Term: Occp Code: Appr Value: Note Date: Debt Ratio: City Zip Code: Purpose: Curr Rate: CLTV: Prin Bal: Maturity Date: Lien Pos: 2576766 WI 301 14 98377 26600 356.25 657 8188002576766 8 252 1 100000 12/18/1996 26 MILLWAUKEE 53219 2 15.750 125 26212.22 01/01/2022 2 3052096 GA 61 9 77155 27660 651.87 670 305209600000000 4 59 1 91000 11/07/2000 36 Gainesville 30507 2 14.570 116 27344.08 12/01/2005 2 3116721 NY 300 14 55000 35000 418.64 688 136990000116721 8 287 1 75000 12/17/1999 45 SYRACUSE 13207 2 13.900 120 34808.43 12/22/2024 2 3200990 MI 122 14 82599 12000 173.17 712 320099000000000 5 119 1 100000 10/31/2000 38 Xxxxxx 48180 2 12.150 95 11896.03 12/01/2010 2 3248971 CA 301 14 78976 60000 768.03 680 106990000248971 8 270 1 115000 06/12/1998 50 HIGHLAND 92346 2 14.990 121 59357.19 07/17/2023 2 3383110 MI 300 14 68437 46500 604.62 671 126990000383110 8 291 1 92000 04/07/2000 46 Dowagiac 49047 2 15.250 125 46370.41 04/19/2025 2 3406126 GA 181 14 49711.8 35000 483.88 675 113990000406126 6 171 1 69000 03/30/2000 39 WARNER ROBINS 31088 2 14.750 123 34111.31 04/04/2015 2 3439641 MI 181 14 129269 40000 597.98 700 126990000439641 6 172 1 173000 04/28/2000 36 Xxxxxxxxxx Xxxxxxxx 00000 2 16.380 98 39347.86 05/02/2015 2 3493133 IN 301 14 112552 35000 421.05 667 118990000493133 8 284 1 118650 08/26/1999 44 Westpoint 47992 2 13.990 125 34772.63 09/15/2024 2 3496170 KY 300 14 134738 34000 485.48 654 349617000000000 8 292 1 135000 05/25/2000 44 LOUISVILLE 40299 2 16.880 125 33946.27 05/30/2025 2 3555993 CA 301 14 157000 75000 888.5 727 355599300000000 8 294 1 220000 06/09/2000 47 Lakewood 90713 2 13.750 106 74820.18 07/01/2025 2 3564781 MA 300 14 111527 35000 513.65 646 356478100000000 8 293 1 140000 06/14/2000 31 Xxxxxxx 1570 2 17.380 105 34949.68 06/19/2025 2 3571147 WV 120 14 63364.64 47200 704.47 727 357114700000000 5 115 1 88500 08/02/2000 35 Martinsburg 25401 2 12.990 125 46263.81 08/07/2010 2 3599309 MD 301 14 212103 50000 517.4 748 359930900000000 8 295 1 250000 07/05/2000 42 Waldorf 20603 2 11.750 105 49858.17 08/01/2025 2 3624830 IN 180 14 81059 20000 275.14 668 000000000000000 6 173 1 90000 06/16/2000 41 Mulberry 46058 2 14.650 113 19808.39 06/21/2015 2 3634217 MO 300 14 48065 35000 404.66 719 363421700000000 8 293 1 70000 06/09/2000 35 Xxxxxxxx 65340 2 13.380 119 34894.63 06/14/2025 2 Page 1 of 409

  • cGMP means current Good Manufacturing Practices as specified in the United States Code of Federal Regulations, ICH Guideline Q7A, or equivalent laws, rules, or regulations of an applicable Regulatory Authority at the time of manufacture.

  • GMPs means the then-current good manufacturing practices required by the FDA, as defined in 21 C.F.R. Parts 210 and 211 and the regulations promulgated thereunder, for the manufacture and testing of pharmaceutical materials, and comparable laws or regulations applicable to the manufacture and testing of pharmaceutical materials in jurisdictions outside the U.S., as they may be updated from time to time. GMPs shall include applicable quality guidelines promulgated under the International Conference on Harmonization.

  • FedRAMP means the Federal Risk and Authorization Management Program (see xxx.xxxxxxx.xxx), which is an assessment and authorization process that federal government agencies have been directed to use to ensure security is in place when accessing Cloud computing products and services.

  • Web Site Accessibility Standards/Specifications means standards contained in Title 1 Texas Administrative Code Chapter 206.

  • MFDA means the Mutual Fund Dealers Association of Canada;

  • Drug means (i) articles or substances recognized in the official United States Pharmacopoeia

  • 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.

  • Federal Regulations means those federal regulations relating to cable television services, 47 C.F.R. Section 76.1 et seq. (and, to the extent applicable, any other federal rules and regulations relating to cable television, including but not limited to, those described in 47 C.F.R. Section 76.3), or as such regulations may be amended.

  • EU Data Protection Law means (i) prior to 25 May 2018, Directive 95/46/EC of the European Parliament and of the Council on the protection of individuals with regard to the processing of Personal Data and on the free movement of such data ("Directive") and on and after 25 May 2018, Regulation 2016/679 of the European Parliament and of the Council on the protection of natural persons with regard to the processing of Personal Data and on the free movement of such data (General Data Protection Regulation) ("GDPR"); and (ii) Directive 2002/58/EC concerning the processing of Personal Data and the protection of privacy in the electronic communications sector and applicable national implementations of it (as may be amended, superseded or replaced).

  • 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).

  • Grid Code / “IEGC” or “State Grid Code” shall mean the Grid Code specified by the Central Commission under clause (h) of sub-section (1) of Section 79 of the Electricity Act and/or the State Grid Code as specified by the concerned State Commission referred under clause (h) of sub-section (1) of Section 86 of the Electricity Act, as applicable;

  • European Data Protection Laws means the EU General Data Protection Regulation 2016/679 (“GDPR”) and data protection laws of the European Economic Area (“EEA”) and their member states and the FADP.

  • Loss Absorption Regulations means, at any time, the laws, regulations, requirements, guidelines, rules, standards and policies relating to minimum requirements for own funds and eligible liabilities and/or loss absorbing capacity instruments of the Kingdom of Belgium, the Relevant Regulator, the Resolution Authority, the Financial Stability Board and/or of the European Parliament or of the Council of the European Union then in effect in the Kingdom of Belgium including, without limitation to the generality of the foregoing, any delegated or implementing acts (such as regulatory technical standards) adopted by the European Commission and any regulations, requirements, guidelines, rules, standards and policies relating to minimum requirements for own funds and eligible liabilities and/or loss absorbing capacity instruments adopted by the Relevant Regulator and/or the Resolution Authority from time to time (whether or not such regulations, requirements, guidelines, rules, standards or policies are applied generally or specifically to the Issuer or to the Group).