Quality Requirements. Performance Indicator Heading Indicator (specific) Threshold Method of Measurement Frequency of monitoring Consequence of Breach
Quality Requirements. Licensee agrees that all Relevant IANA Services offered under the Licensed Marks shall be of a consistent quality at least as high as the quality of comparable services offered by ICANN immediately prior to the Effective Date and shall comply with the service quality requirements contained in the Service Agreement. Licensor and Licensee agree that quality monitoring responsibilities hereunder shall be conducted by the Relevant Community, which shall report any failure of the Relevant IANA Services to comply with the relevant quality standards to Licensor.
Quality Requirements. Supplier shall comply with Tesla’s quality requirements set forth in Attachment 6 entitled “Tesla Motors Supplier Handbook”.
Quality Requirements. 5.5.1. Each assignment shall be carried out in full and as accurately as possible in accordance with the instructions given in the order form. The work delivered shall have been thoroughly revised and checked by the Contractor, so as to be usable, as it stands, without further revision by the Translation Centre. The Contractor shall pay particular attention to ensuring that all references to documents already published have been checked and cited correctly, that any documentation referred to in Article 5.9 has been consulted, and that the terminology used is consistent throughout the text. Where an assignment is returned incomplete, the Contractor shall be obliged, when asked, to make good any omissions.
5.5.2. The Contractor may be asked to provide a definitive version of an assignment incorporating corrections made by the Translation Centre. This work shall be carried out within a reasonable time period and shall not give rise to any additional remuneration for this service.
Quality Requirements. The Contractor shall be required to demonstrate by means of a Quality Plan that this organisation is so structured that all the requirements of the specification will be properly monitored and controlled. The Quality Plan and Control procedures are to be carried out in accordance with the Quality Control document NWS 1841/C1 and the Matla Quality Manual for Contractor. The Quality Control document is to be submitted for approval to Matla Engineering within three (3) days after order placement by the Contractor. No work may commence unless the Quality Control document has been approved in writing and a copy submitted to the Employers Representative. The Contractor, in conjunction with Matla Engineering must sign off all Quality Control documents after completing all work on site. The Contractor to submit a copy of the final signed off document to the Employers Representative within 1 week after Completion of a Unit.
Quality Requirements. Customer represents and warrants to Owner that all Biomass tendered by or for the account of Customer for Terminal Services will conform to the Specifications. Owner will not be obligated to load or unload Biomass that fails to meet the Specifications at the time tendered by Customer, but, to the extent that Owner loads or unloads Biomass that fails to meet the Specifications, in no event will Owner have any liability whatsoever for loading or unloading such Biomass. Owner may, upon prior written notice to Customer, impose other limitations on the Biomass delivered to the Terminal in order to (a) comply with applicable Laws, (b) protect health and safety, and (c) protect the premises, equipment or facilities at the Terminal.
Quality Requirements quality of the Contract Commodity shall correspond with design documentation (drawings, specifications or other technical documents) and the Technical Agreement signed jointly by the Buyer and the Seller. In the event of any irrationality in aforementioned design documentation, the Seller shall within 3 days from the date of discovery inform the Buyer in a written notice.
Quality Requirements. The following quality requirements also apply to CPAM Services:
Quality Requirements. The Supplier acknowledges and agrees that:
(a) all Goods and any Services must conform to and meet all applicable specifications, drawings and descriptions set out in Schedule A – Scope of Supply and all other requirements of this Contract;
(b) unless otherwise stated in this Contract, all Goods must be of good quality, new and undamaged;
(c) the Goods must be free from defects in design, materials and workmanship at the time the Goods are received at the Delivery Location;
(d) the Goods must be fit and suited for Moose Jaw's purpose and use specified in this Contract; and
(e) any Services must be performed in accordance with prudent industry standards for services of a similar nature, having regard to the requirements of this Contract.
Quality Requirements. 8.1 Clozapine must only be provided once a satisfactory blood result has been received.
8.2 Prescription Forms for clozapine must be written by a qualified Prescriber.
8.3 The Provider acknowledges and agrees that the prescribing and Dispensing of clozapine is subject to restrictions issued by Te Whatu Ora – Health New Zealand, including the requirement for blood monitoring.
8.4 In order to be qualified to provide Clozapine Services, the Provider must:
(a) have read, and be able to comply with, this Service Schedule and the Clozapine Protocol;
(b) ensure that relevant Staff have completed the questionnaire on the Dispensing of clozapine and submitted it to the relevant pharmaceutical supplier; and
(c) ensure that relevant Staff have attended regular training on the Dispensing of clozapine at least annually, and record that this has occurred. The training package and records must be available for audit purposes.
8.5 The ability to comply with the requirements in clauses 8.4(b) and 8.4(c) above is dependent on the questionnaire and training session being developed and made available to providers by Te Whatu Ora – Health New Zealand.
8.6 Clozapine Services must only be provided by a Pharmacist that complies with the requirements specified in clause 8.4(a) and has completed the questionnaire, training and annual validation sessions and recording, detailed in clauses 8.4(b) and 8.4(c), when these are available to providers.
8.7 The Provider is responsible for the management of Clozapine Services at all times.
8.8 The Provider must comply with any quality requirements set out in the Clozapine Protocol.
