Product Specifications. The Company agrees that all Products sold to Xxxx hereunder shall conform to the respective specifications set forth on Schedule A or to such other specifications as are from time to time agreed upon by the Parties.
Product Specifications. (a) Supplier shall manufacture all Products according to the Specifications in effect as of the date of this Agreement, with such changes or additions to the Specifications of the Products related thereto as shall be requested by Buyer in accordance with this Section or as otherwise agreed in writing by the Parties. All other Products shall be manufactured with such Specifications as the Parties shall agree in writing.
(b) Buyer may request changed or additional Specifications for any Product by delivering written notice thereof to Supplier not less than one hundred twenty (120) days in advance of the first Firm Order for such Product to be supplied with such changed or additional Specifications. Notwithstanding the foregoing, if additional advance time would reasonably be required in order to implement the manufacturing processes for production of a Product with any changed or additional Specifications, and to commence manufacture and delivery thereof, Supplier shall so notify Buyer, and Supplier shall not be required to commence delivery of such Product until the passage of such additional time.
(c) Supplier shall be required to accommodate any change of, or additions to, the Specifications for any Product, if and only if (i) in Supplier’s good faith judgment, such changed or additional Specifications would not require Supplier to violate good manufacturing practice, (ii) the representation and warranty of Buyer deemed made pursuant to Subsection (e) below is true and correct, and (iii) Buyer agrees to reimburse Supplier for the incremental costs and expenses incurred by Supplier in accommodating the changed or additional Specifications, including the costs of acquiring any new machinery and tooling. For the avoidance of doubt, such costs and expenses shall be payable by Buyer separately from the cost of Products at such time or times as Supplier shall request.
(d) Supplier shall notify Buyer in writing within thirty (30) days of its receipt of any request for changed or additional Specifications (i) whether Supplier will honor such changed or additional Specifications, (ii) if Supplier declines to honor such changed or additional Specifications, the basis therefor and (iii) if applicable, the estimated costs and expenses that Buyer will be required to reimburse Supplier in respect of the requested changes or additions, as provided in Subsection (c) above. Buyer shall notify Supplier in writing within fifteen (15) days after receiving notice of any requi...
Product Specifications. (a) Each Product to be offered for trading through the Exchange will be defined by a Product Specification.
(b) Product Specifications will be determined by the Operator from time to time after consulting with Trading Participants in accordance with clause 3, and will be incorporated into and form part of this Agreement.
Product Specifications. Each Product delivered by Lessee into storage or by Lessor from storage must meet the respective specifications set out in Exhibit “A” attached hereto and made a part hereof. Lessor reserves the right to modify, add to, or revise such specifications at any time and from time-to time upon giving not less than thirty (30) days prior written notice.
Product Specifications. The parties shall consult with each other in establishing Product specifications; provided, however, that all Product specifications shall be finally determined by Nomaco in Nomaco's sole discretion, after consultation with RBX.
Product Specifications. A certificate of analysis shall accompany each shipment of the MSD Compound to Collaborator. Upon request, Collaborator shall provide MSD with a certificate of analysis covering each shipment of Collaborator Compound used in the MSD Compound Study.
Product Specifications. Product supplied to Celltech by Orphan Medical shall meet the Product Specifications that are approved by the Regulatory Authorities in the Territory. Should the approved Product Specifications differ from the specifications contained in Orphan Medical’s NDA which are set forth on Appendix C, the Product Specifications approved by the Regulatory Authorities shall control.
Product Specifications. The products and materials to be provided must meet the performance and technical requirements of the Contract Documents. Provide products complete with accessories, trim, finish, fasteners, and other items needed for a complete installation and indicated use and effect. If available, and unless custom products or non-standard options are specified, provide standard products of types that have been produced and used successfully in similar situations on other projects. The Commission reserves the right to limit selection to products with warranties that do not conflict with the requirements of the Contract Documents. Where products are accompanied by the term “as selected,” the Authorized Commission Representative will provide the selection. Where products are accompanied by the term “match sample,” the sample to be matched is that provided by the Authorized Commission Representative. Where products are specified by name and accompanied by the term “or equal,” or “or approved equal,” or “or approved,” the product proposed by Design-Builder must be approved by the substitution process set forth in Section 13.06 below.
Product Specifications. “Product Specifications” shall mean the specifications for the Product which will be attached hereto as Exhibit 5 and made a part hereof, as determined in accordance with the analytical methodology agreed upon by the Parties, as such specifications may be amended from time to time by mutual agreement of the Parties, including without limitation such amendments as may be required to obtain Product Approval.
Product Specifications. All Offerors responding must provide detailed device specifications demonstrating their ability to meet or exceed the listed criteria, or provide a justification as to why alternate specifications should be considered. The State will deem any response that does not meet the specifications listed below without providing adequate justification for an alternate bid non-responsive. Additionally, Offerors should classify products as Class 1 – Having No Medical Training or Class 2 – Slight Medical Training, and any other classes as appropriate. Offerors should include the cost associated with each device being bid separately using the provided Cost Proposal Forms (Attachment C). If cost information is provided outside of the separate cost proposal section, the Lead State reserves the right to redact an Offeror’s proposal so that it complies with the requirements of the RFP. Such redaction may have a detrimental effect on the competitiveness of an Offeror’s Proposal.
a. Public Access and Infrequent User AEDs
i. The AED must enhance user performance by displaying visual icons or audible prompts.
ii. The AED must guide the rescuer in following the proper rescue sequence.
iii. The AED must utilize a biphasic waveform with maximum energy setting of 200 Joules.
iv. The AED must be user configurable to adapt to local and changing protocols.
v. The AED must be capable of automatic self-tests of the internal circuitry delivery system.
vi. The AED self-tests perform automatic daily self-tests or be user programmable for 1-7 day time intervals.
vii. The AED must offer the capability of a user-activated manual selftest.
viii. The AED must include an easily identifiable on/off switch on the front of the device.
ix. The AED must have an easy to see status indicator that advises users if the unit requires service.
x. The AED must offer an audible tone that sounds if the unit requires service.
xi. The AED must record data to an internal memory.
xii. The AED must include the ability to download data to a computer.
xiii. The AED must utilize pre-connected, disposable, single use, selfadhesive electrode(s).
xiv. The electrode must have a shelf life of at least two years.
xv. The AED must have a cable length of at least 48 inches.
xvi. The AED must include a patient analysis system that automatically evaluates patient ECG or shockable/non-shockable rhythms.
xvii. The AED must be able to operate in a temperature range of 32 degrees Fahrenheit to 122 degrees Fahrenheit.
xviii. The AE...
