Examples of Portal Measurement Products in a sentence
Under the terms of the Agreement, the Parties acknowledge and agree that the ownership of the Intellectual Property in certain Products and the Portal Measurement Products shall be as set forth on Exhibit 6.1. Nothing in Exhibit 6.1 shall imply any further commitment by either party under this Amendment to develop the C-BAM or X-BAM.
The following Schedules form an integral part of this Manufacturing Agreement: Schedule 1: Required Quality Data Schedule 2: Portal Measurement Products and Specifications Schedule 3: Philips Terms of Delivery Schedule 4: Prices/Quantities Schedule 5: Contact Persons Schedule 6: Cosmetic Defect Guideline Schedule 7: Cosmetic Inspection Guideline DIAMETRICS MEDICAL, INC.
Reasonable attempts by Philips 1st Level Application Support (Response Centers) to determine failure mode(s) of the Portal Measurement Products is assumed.
Philips shall issue binding written purchase orders for Portal Measurement Products at least sixty (60) days prior to the proposed shipping date for such items.
Diametrics shall manufacture the Portal Measurement Products with material purchased directly by Diametrics.
Both Parties shall appoint additional contact persons in Schedule 5 to facilitate communication regarding specific aspects of the manufacture and supply of the Portal Measurement Products hereunder.
Diametrics agrees to provide commercially reasonable support to Philips, at Philips' written request and at Philip's expense, as required to meet United States and international environmental laws, regulations and standards applicable to the manufacture of the Portal Measurement Products.
This Manufacturing Agreement stipulates the additional terms and conditions for the supply of Portal Measurement Products to Philips by Diametrics, including any Portal Measurement Products supplied by Diametrics prior to or during the Term hereof.
Diametrics shall retain records of any safety, quality and reliability related data relating to the Portal Measurement Products as well as any data necessary for "Current Good Manufacturing Practices" (CGMP, as required by FDA), the "In Vitro Diagnostics Directive" (the IVDD, as required by the European Union) and the "Medical Device Directive" (MDD, as required by the European Union), to the extent provided under Schedule 1, Required Quality Data.
This information will be transferred to Diametrics prior to any Portal Measurement Products being returned from the field.