GMPP definition

GMPP means this CSG Group Management Performance Plan as set out herein, as from time to time amended.
View Source
GMPP means the Government Money Purchase Pension Plan created by the Government Money Purchase Pension Plan Act, RSNL 1990, c G-6, as amended from time to time, and the regulations issued thereunder.
View Source
GMPP means the guaranteed maximum plant price, which shall consist of the GMP, Development Costs, Construction Financing Costs, Other Costs, and Financing Costs, and shall be determined in accordance with Exhibit B, including the caps for specific elements of the GMPP set forth therein.
View Source

Examples of GMPP in a sentence

  • Continuation /participation in the GMPP or PSPP will be in accordance with established Pension Regulations and guidelines.

  • Source Atlantic can provide a variety of procurement services from basic support of the existing materials and purchasing team to accepting the associated risks by purchasing the equipment via our “Guaranteed Maximum Pricing Program” (GMPP).

  • The Institute will also need to contribute to the Department’s quarterly GMPP returns, to enable effective budget monitoring against the published objectives of the apprenticeship and technical education programmes.

  • The sales consultant will participate in the gross on GMPP sales as per our GMPP Minimum Standards Plan.

  • This GMPP Sales Consultant plan is subject to change if performance is not satisfactory and/or changes from GMPP.

  • The Employer agrees that all new employees who are eligible shall become and remain members of either GMPP or the Public Service Pension Plan.

  • Schedule 1.1 Acquired Assets Schedule 1.2 Specified Excluded Assets This BILL OF SALE, ASSIGNMENT AND ASSUMPTION AGREEMENT is entered into as of April 29, 2025, (the “Execution Date”) by and among, Authentic Holdings, Inc., a Nevada corporation (“Buyer”), Goliath Motion Picture Promotions a sole proprietorship (“GMPP”) and Pr▇▇▇▇▇▇▇ ▇▇▇▇▇▇, an individual (“Co▇▇▇▇”) and the sole owner of GMPP (collectively, GMPP and Co▇▇▇▇ ▇re hereinafter referred to as the “Seller”).

  • The GMPP Program changes every year beginning with the calendar year, as of January 1, 2001.

  • There is a requirement to co-ordinate multiple workstreams, delivery across various suppliers, internal / external de- pendencies and key stakeholders, alongside external governance, and con- trols as part of GMPP IPA and HMT reviews, and the delivery of extensive business change.

  • Upon doing so, the business office also informs the buyers of our Customer Satisfaction Program which is made up of GMPP, PERSONALIZED NORTHERN ONTARIO SERVICE PROGRAM, GM CSi PROGRAM and our CUSTOMER FOR LIFE mission.

Related to GMPP

  • 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.

  • 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.

  • 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.

  • cGCP means the then current Good Clinical Practices that establish the national and international ethical and scientific quality standards for designing, conducting, recording and reporting clinical trials that are promulgated or endorsed for the United States by the FDA (including through ICH E6 and 21 CFR Parts 50, 54, 56 and 312) and for outside the United States by comparable Governmental Authorities.

  • Participating Clinical Laboratory means a Clinical Laboratory which has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.