Initial samples and requalification Sample Clauses

Initial samples and requalification. The manufacturing and test conditions must be agreed to during the launch phase of a program, for all parts without initial sampling process prior to the deliveries first. If initial samples are ordered by ISH, the SUPPLIER must punctually submit the agreed amount of manufactured initial samples including the documentation for the samples before commencing batch production under series conditions. An advanced sampling strategy agreement is part of the initial sampling process. The plan must be documented in specific product related quality requirements as an appendix of the general overall quality agreement. The measurement methods and measuring equipment must be coordinated with ISH in advance in order to guarantee comparability. Series production may only be commenced after approval by ISH. In cases where ISH can not approve initial samples due to issues caused by the supplier (e.g. incomplete fulfilment of the approved sampling strategy agreement) the SUPPLIER will be charged according to expenditure. Expenses incurred as by complete or partial repetition of the sampling process. The supplier undertakes to deliver as quickly as possible to free replacement. The requirements of sampling plan, the SUPPLIER receives as part of the initial sample order. The SUPPLIER is obliged to ensure for production and service deliveries each year of delivery a complete requalification test. The SUPPLIER will document the complete requalification with the submission of a complete initial sample report (incl. dimensional accuracy, material confirmation, reliability tests, conformity to legal and environmental standards) according ISO TS 16949.
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Initial samples and requalification. Unless otherwise agreed, samples of new parts shall be provided together with an initial sample inspection report in accordance with VDA (German Association of the Automotive Industry) 2 "Assuring the Quality of Supplies", Sample Stage 2. Initial samples must be manufactured entirely using series equipment and under series conditions. The Supplier shall fulfil all specifications in accordance with the drawing, technical terms of delivery, standards etc. If the Supplier is unable to carry out individual tests itself, it must allocate them to a suitable testing centre. Responsibility shall always remain with the Supplier. Once the initial samples and the fully completed initial sample inspection report (ISIR) have been presented, ETG/XXXXX shall, at its own discretion, carry out counter- testing to check actual values. The evaluated ISIR shall be returned to the Supplier without delay. The Supplier shall be able, on request, to produce initial samples to meet VDA Level 2 or PPAP Level 3 and to make an entry in the IMDS.

Related to Initial samples and requalification

  • Professional Qualifications It shall be a condition of continued professional employment that employees must apply for enrolment in their appropriate professional licensing body by the thirtieth day of continuous service.

  • Contractor Qualifications Contractor warrants that Contractor has the necessary licenses, experience and technical skills to provide services under this Contract.

  • Designated Prescription Drug Prescribers and Pharmacies We may limit your selection of a pharmacy to a single pharmacy location and/or a single prescribing provider or practice. Those members subject to this designation include, but are not limited to, members that have a history of: • being prescribed prescription drugs by multiple providers; • having prescriptions drugs filled at multiple pharmacies; • being prescribed certain long acting opioids and other controlled substances, either in combination or separately, that suggests a need for monitoring due to: o quantities dispensed; o daily dosage range; or o the duration of therapy exceeds reasonable and established thresholds. The Amount You Pay for Prescription Drugs Our formulary includes a tiered copayment structure, which means the amount you pay for a prescription drug will vary by tier. See the Summary of Pharmacy Benefits for your copayment structure, benefit limits and the amount you pay. When you buy covered prescription drugs and diabetic equipment and supplies from a retail network pharmacy, you will be responsible for the copayment and deductible (if any) at the time of purchase. You will be responsible for paying the lower of your copayment, the retail cost of the drug, or the pharmacy allowance. Specialty prescription drugs are generally obtained from a specialty pharmacy. If you buy a specialty prescription drug from a retail network pharmacy, you will be responsible for a significantly higher out of pocket expense than if you bought the specialty drug from a specialty pharmacy. The amount you pay for the following prescription drugs is not subject to the tiered copayment structure: • Contraceptive methods; • Over-the-counter (OTC) preventive drugs; • Nicotine replacement therapy (NRT) and smoking cessation prescription drugs; • Infertility specialty prescription drugs; and • Covered diabetic equipment or supplies bought at a network pharmacy. See the Summary of Pharmacy Benefits for benefit limits and the amount you pay. This plan allows for medication synchronization in accordance with R.I. General Law

  • Preferred Provider - Prescription Drugs The Board shall provide, through the Xxxxx County Council of Governments, a preferred provider drug program that, if the employee chooses to utilize, will include the following:

  • Proposing Integration Activities in the Planning Submission No integration activity described in section 6.3 may be proposed in a CAPS unless the LHIN has consented, in writing, to its inclusion pursuant to the process set out in section 6.3(b).

  • Personnel Qualifications Contractor shall assign properly qualified and experienced personnel to the program contemplated under this Agreement, and Contractor shall use reasonable efforts to retain such personnel on Customer’s program for the duration of such program.

  • Statistical Sampling Documentation a. A copy of the printout of the random numbers generated by the “Random Numbers” function of the statistical sampling software used by the IRO.

  • Demographic, Classification and Wage Information XXXXXX agrees to coordinate the accumulation and distribution of demographic, classification and wage data, as specified in the Letter of Understanding dated December 14, 2011, to CUPE on behalf of Boards of Education. The data currently housed in the Employment Data and Analysis Systems (EDAS) will be the source of the requested information.

  • Evaluation Cycle: Formative Assessment A) A specific purpose for evaluation is to promote student learning, growth and achievement by providing Educators with feedback for improvement. Evaluators are expected to make frequent unannounced visits to classrooms. Evaluators are expected to give targeted constructive feedback to Educators based on their observations of practice, examination of artifacts, and analysis of multiple measures of student learning, growth and achievement in relation to the Standards and Indicators of Effective Teaching Practice.

  • Promotions Requiring Higher Qualifications Consideration for promotion shall be given to the senior applicant who does not possess the required qualifications but is presently obtaining such qualifications prior to filling the vacancy. At the discretion of the Employer, such an employee may be given a trial period to qualify within a reasonable length of time and will revert to her former position if the required qualifications are not met within such time.

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