Validation Testing. Oracle shall review the integration of your application program with the Oracle application programs (“Integration Validation Assistance”) for the purposes of accepting it as a validated integration (the “Validated Integration”). Oracle shall only commence the Integration Validation Assistance once the applicable integration validation testing application and validation test plan have been completed by you, have been reviewed and accepted by Oracle (the “Validation Test Plan”) and the applicable fee has been received by Oracle. You shall submit a validation testing application within 60 days of the effective date of this Addendum. For each application program that you request Oracle to review during the term of this Addendum, you shall submit a separate validation testing application and Validation Test Plan. The Validation Test Plan template that you must use is available at the Oracle PartnerNetwork web site at xxxx://xxxxxxx.xxxxxx.xxx (log in, select Membership / Agreements & Policies). Integration Validation Assistance is comprised of a test plan and testing review, integration process and methodology review, and validation of the integration for the specific version of your applications program indicated in the Validation Test Plan and for the specific version of the Oracle applications programs indicated in the Validation Test Plan. You acknowledge that Oracle’s ability to provide you with Integration Validation Assistance is dependent on your timely cooperation including, but not limited to, your providing Oracle with access to your application and other resources including a non-production instance of your application and the applicable Oracle application available on your network. Integration Validation Assistance is a “service” as defined in the Agreement. In the event that Oracle is unable to accept the integration of your application program as a Validated Integration, then you may re-submit the application program for review which may be subject to an additional fee as set forth below. Applications Integration Kit Oracle shall grant you a non-exclusive, non-transferable, limited license to use the Oracle applications integration tool kit specified in the Validation Test Plan comprising integration development guides, online integration workshop(s) and such other upgrades, new releases, software or services as may be made generally available by Oracle from time to time (the “Applications Integration Kit”). The Applications Integration Kit is...
Validation Testing. This will be system testing, in participating schools, that confirms that the solution meets or exceeds the functional requirements, and the performance and reliability specifications as required under the Agreement between the Provider and the Department resulting from this procurement process. This Validation Test will enable the Provider the opportunity to test its equipment in school environments and will assure the Department that the solution is acceptable for production deployment. The test will include up to five (5) schools and must be successfully completed by July 19, 2013.
Validation Testing. In conjunction with the Company, identify and work with leaders in the medical fields served by the New Product at teaching hospitals and universities to determine the need for the New Product and the required validation and clinical trials to determine its feasibility and efficacy. Design and participate in validation testing of the New Product to determine whether the prototype device is able to perform the functions described in paragraph 1.a with respect to that New Product.
Validation Testing. Each party shall provide commercially reasonable levels of resources necessary to validate DICOM connectivity and verify clinical usability after each Update, Upgrade or New Feature, if any.
Validation Testing. CLIENT shall test Software, using QCSI's hardware and Software and CLIENT's data ("Validation Test"), that Software performs according to Documentation (as defined in the QCSI Quality Commitment Guide, which is incorporated herein by reference) and Exhibit B, "Success Criteria". CLIENT will initiate Validation Test no later than six (6) months (unless there is mutual agreement by both parties herein) after the effective date of this License and the Validation Test will be limited to no more than [****] ("Test Period"). If the Software is performing according to the Documentation and Exhibit B, CLIENT will provide QCSI with written acceptance within ten (10) days after the end of the Test period. If the Software does not perform according to the Documentation, CLIENT will provide to QCSI a written summary of any anomalies within ten (10) days at the end of the Test Period. If such summary of anomalies is not received within ten (10) days after the end of the "Test Period", it shall be interpreted as acceptance of the Software by CLIENT. QCSI will have [****] in which to respond to any anomalies from the Documentation. If such anomalies from the Documentation are not corrected within a [****] time period, this shall constitute material breach of this License.
Validation Testing. 5.1.6.1 Validation Test Plan - The Government will provide a formal Test Plan to the Contractor prior to each required test event to define the validation requirements and pass/fail/retest criteria for the event.
Validation Testing. Upon completion and approval of TRR, the Government will perform formal validation testing in accordance with Test Plan. The Contractor shall generate Test Incident Reports (TIR) for each discrepancy identified by the Government during testing. These TIRs shall be submitted to the Government on completion of testing and will be used by the Government to track the Contractor’s resolution of all issues identified. The Government will conduct follow-on validation, as required, to ensure that all discrepancies are corrected.
Validation Testing. 1.1 Manufacturer shall design and conduct, or procure the design and conduct of all validation testing of Manufacturing equipment and/or procedures where this is required for the sole purpose and necessity of maintaining Product registrations in the US, the UK, the EU and Rest of World. For the avoidance of doubt, this shall include additional validation work related to the Manufacturing equipment and/or Manufacturing procedures required for any necessary upgrading of Product dossiers to meet UKCA Xxxx and/or EU MDR and/or US Food and Drug Administration (“FDA”) requirements or other changes in applicable regulatory requirements in these jurisdictions or in the Rest of World.
Validation Testing. IMPCO may assist the JVC in getting quotations from itself and from its Affiliates for equipment and components. IMPCO and MXXXX agree to assist the JVC in adopting the most economical methods of procurement. IMPCO may l make available to the JVC the services of its international marketing and distribution network and of its Affiliates. IMPCO will provide, on the basis of a program to be mutually agreed with the Parties as to people and time, training to the JVC personnel in various fields like manufacturing, design, quality, testing, etc. IMPCO will not charge any cost from the JVC. However, all the travelling, boarding and lodging expenses of the personnel of MXXXX IMPCO Limited will be borne by the JVC.
Validation Testing. The Product is “off-the-shelf” which assumes all validation testing is acceptable and complete. Additional testing or requirements must be negotiated and mutually agreed upon. PARTIALLY REDACTED PURSUANT TO CONFIDENTIAL TREATMENT REQUEST
