Product Qualification Sample Clauses
The Product Qualification clause defines the standards and procedures that a product must meet before it can be accepted or used under the agreement. Typically, this involves specifying technical requirements, testing protocols, or certification processes that the product must undergo to demonstrate compliance. For example, a supplier may need to provide test results or certifications showing that their product meets industry safety standards. The core function of this clause is to ensure that only products meeting agreed-upon quality and safety criteria are delivered, thereby reducing the risk of defects and ensuring reliability for the buyer.
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Product Qualification. LICENSEE will not sell, or otherwise distribute, a LICENSEE product under HP’s Trademarks as provided in this Agreement until the following requirements have been performed to meet HP’s requirements: 1) qualification reports delivered and presented to the HP Program Manager; and, 2) LICENSEE has received approval from HP for product release. LICENSEE will make, or have made, the HP Branded Products in a way that meets or exceeds the performance and Quality Standards as defined in the product specification, which may be amended by written agreement from time to time. LICENSEE will perform, and fund, the cost of product qualification according to these specifications. These specifications and requirements would include, but not be limited to, the following:
Product Qualification. The process of validation and verification that the product meets all defined Engineering and Quality requirements.
Product Qualification. The Supplier and EVVA Sicherheitstechnologie agree to a joint qualification programme in good time before the deliveries. The products must correspond to the agreed or assured characteristics (e.g. specifications, data sheets, drawings, samples). The Supplier shall check immediately whether a description provided by EVVA Sicherheitstechnologie (e.g. specification, specifications sheet, data sheets, drawings) are obviously faulty, unclear, incomplete or obviously deviate from a possible sample. If the Supplier recognises that this is the case, they will immediately notify EVVA Sicherheitstechnologie in writing before commencing with the production process or providing the service. After qualification, the Supplier will not introduce any changes to the product and/or significant changes to the production process without timely prior notification of EVVA Sicherheitstechnologie, see Clause 11 (“Change control”). EVVA Sicherheitstechnologie reserves the right to reject deliveries and is entitled to restart the qualification process if it has been substantiated that products do not fulfil the requirements.
Product Qualification. Qualification timeline and activities will be added to the agreement upon identification of B▇▇▇▇’s [***] in accordance with Clause 5.1.
Product Qualification. TI's written certification that TI Products and their manufacture have achieved a level of quality, consistency and reliability that meets or exceeds the Specifications in accordance with this Agreement.
Product Qualification. (a) NXP shall perform Product qualifications in accordance with the Specifications.
(b) NXP shall release diffusion processes in accordance with NXP’s procedure SNW-SQ-020 set forth in Annex I and shall release new packages in accordance with NXP’s procedure SNW-FA-03-04 in Annex I.
Product Qualification. OGC shall afford the Sellers the opportunity to qualify to manufacture and sell all Films ordered by OGC as follows:
(a) First, the Sellers must inform OGC in writing as to the Films they intend to offer to manufacture and sell to OGC, together with the prices to be charged to OGC for such Films, delivery terms, specifications and other material conditions. OGC shall then promptly determine whether the price and other terms and conditions are at least as favorable (equal) as those offered by OGC's and other available suppliers. If the Sellers fail to inform OGC in writing as to any particular Film they intend to offer to manufacture and sell to OGC within 30 days following their receipt of the information and physical sample with respect to such Films as set forth in Section 2 above, then OGC shall have no obligation to allow the Sellers to qualify such Film under this Section 3 or to purchase any specified quantities thereof as set forth in Section 4 below. In the event that the Sellers desire to, and are subsequently able to, offer and manufacture any Films at a later date, then OGC shall give the Sellers an opportunity at a mutually convenient time or times during the term of this Agreement to qualify such Films pursuant to this Section 3.
(b) Second, once the parties agree that the price and other terms are at least as favorable as those offered by OGC's and other available suppliers and further agree on the price and other terms for the Films to be supplied by the Sellers to OGC, the Sellers shall produce a sample order for the Films, and OGC shall inspect such order for competitive quality and compliance with OGC's specifications. As used herein, the term "Acceptable Quality" shall mean Films demonstrating quality competitiveness and compliance with industry norms, applicable legal requirements and OGC's specifications (within reasonably acceptable tolerances and variations as are customary and normal in the industry). If the sample order demonstrates Acceptable Quality, then the parties shall adhere to the supply levels set forth in Section 4(a) below.
Product Qualification. Product qualification is [***], with [***] defined in section [***]. In addition, the [***] will need [***] the quantity of [***] required for this task.
2.1.10.1 Product Qualification Test List 1 [***] [***] [***] [***] [***] [***] 2 [***] [***] [***] [***] [***] [***] 3 [***] [***] [***] [***] [***] [***] 4 [***] [***] [***] [***] [***] [***] 5 [***] [***] [***] [***] [***] [***] 5 [***] [***] [***] [***] [***] [***] 1 [***] [***] [***] [***] [***] [***] 2 [***] [***] [***] [***] [***] [***] 3 [***] [***] [***] [***] [***] [***] 4 [***] [***] [***] [***] [***] [***]
5.1 [***] [***] [***] [***] [***] [***]
5.2 [***] [***] [***] [***] [***] [***]
5.3 [***] [***] [***] [***] [***] [***] NOTES:
1. For [***], [***] will test each [***] separately for [***] samples. One would need at total of [***] for a device with [***] power groups for each of the [***] tests.
2. [***] Test conditions of [***] should be used as [***] for the [***] and not a [***].
3. [***] — Maximum [***]
4. [***] is selected based on estimated [***] of the part at [***], at a [***] of [***].
5. [***] will be done on [***] or [***] units only.
6. [***] will done on [***] units from each of [***] the [***] test to look for possible [***].
7. [***] is not recommended for [***]. [***] is the recommended [***] and is required for [***] instead of [***].
8. [***] of the [***] test will be preformed, [***], is required, [***]. [***] recommends [***] for [***] & [***] for [***]. Must be run at [***]. If the part [***] during the [***] is greater than [***], [***] is recommended.
9. [***] units will be used as part of all [***].
10. [***] would follow the latest JDEC recommended [***] and [***] latest specification, at the time the qualification process starts.
11. The [***] will be submitted to the customer and needs to be approved before we can start ordering the qualification hardware.
12. [***] will be performed using [***]. Quantity of [***] with [***] will be designed and manufactured. The [***] will be done in series unless additional [***] are ordered by the customer.
13. All of the [***] may be done in parallel if we [***] as [***] separate assembly lots [***].
2.1.10.2 Product Qualification Hardware Qualification will be performed using [***] for this purpose. Quantity of [***] with [***] will be designed and manufactured.
2.1.10.3 Product Qualification Environmental Stress Test [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [**...
Product Qualification. Testing (PQT) shall be performed and documented to demonstrate product/process conformance to customer requirements. -------------------------------------------------------------------------------- DATE: November 1993 NPI QUALITY MANUAL SECTION: 4.4 ISSUE: A REVISION: 0 --------------------------------------------------------------------------------
Product Qualification. Eastman will validate the process to produce SAIB [* * *] and file a DMF with the U.S. Food and Drug Administration (“FDA”) (as further defined below) on or about [* * *] after the Effective Date of this Agreement provided that payments as outlined in Section 2.4, Cost Recovery have been completed as outlined in Section 2.4. This timeline shall be extended if [* * *]. In the case of [* * *]. Prior to [* * *]. Commencing from the time of [* * *]. Furthermore, third parties which have a contractual relationship with Durect for use of Product (“Durect Licensees”) shall also be allowed to [* * *] provided that in Durect’s contract with such Durect Licensee, such Durect Licensee provides to Durect acknowledgements, representations, warranties and indemnities no less stringent than provided by Durect to Eastman under Article 7 herein and such Durect Licensee shall be subject to terms relating to the disclosure and use of confidential information no less stringent than applicable to Durect in Article 9 herein.