DESCRIPTION OF REAGENT Sample Clauses

DESCRIPTION OF REAGENT. Reagent shall mean the materials of the same type and nature provided by Supplier to Customer during the months of October and November, 2002, being the compounds referred to as CPO1 and CPO2, and sometimes together known as PEVA/PBMA. ** CONFIDENTIAL TREATMENT REQUESTED ATTACHMENT B REAGENT SPECIFICATIONS Reagent Specifications shall mean the specifications pursuant to which Customer accepted Reagent provided by Supplier during the months of October and November, 2002, except as the parties may otherwise hereinafter agree by written document executed by authorized personnel of each of Supplier and Customer. Such Specifications in effect for the Reagent Supply during October and November, 2002 are described as follows: 2. CONFIDENTIAL TREATMENT REQUESTED ATTACHMENT C ** TARGET PRODUCTION IN KILOGRAMS ** TARGET PRODUCTION (IN KILOGRAMS) ------------------------------- ---------------------------- ---------------------------- ------------------------------- ---------------------------- ---------------------------- ------------------------------- ---------------------------- ---------------------------- ------------------------------- ---------------------------- ---------------------------- ------------------------------- ---------------------------- ---------------------------- ------------------------------- ---------------------------- ---------------------------- ------------------------------- ---------------------------- ---------------------------- ------------------------------- ---------------------------- ---------------------------- ------------------------------- ---------------------------- ---------------------------- ------------------------------- ---------------------------- ---------------------------- ------------------------------- ---------------------------- ---------------------------- ------------------------------- ---------------------------- ---------------------------- ------------------------------- ---------------------------- ---------------------------- ------------------------------- ---------------------------- ---------------------------- ------------------------------- ---------------------------- ---------------------------- ------------------------------- ---------------------------- ---------------------------- **. ** CONFIDENTIAL TREATMENT REQUESTED ATTACHMENT C-2 REAGENT PRICING The purchase price of Conforming Reagent shall be as follows in respect of amounts of Conforming Reagent delivered during each such calendar ...
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Related to DESCRIPTION OF REAGENT

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  • Labelling The distributor, on behalf of the selected vendor agrees that all supplies of articles should invariably contain the following information on its label and the carton. One information should not be overlapped by any other information needed to be furnished. The label should contain : a. Name of the item as approved b. CMS Cat. No. c. Manufacturing date/Import date for the imported items. d. Expiry Date. (where applicable) e. Name & address of Registered Office of Manufacturers and place of manufacture. f. Manufacturing License Number. (where applicable for Manufactures) g. Batch Number (where applicable) h. Month and Year of supply. i. The label & Carton must invariably marked “W B. GOVT SUPPLY : NOT FOR SALE”. j. All Surgical items quoted/supplied by the tenderer must conform to IS /BIS /CE/USFDA. Pacemker must conform to CE & US FDA norms. In case of Drugs items quoted /supplied by tenderer MUST CONFORM TO IP, BP, or USP norms and N.F.I. –III specification as noted against the item(s) in catalogue as applicable. k. The MRP and Trade Name will not be allowed to be printed in any pack. This will lead to cancellation of candidature straightaway. However, for excisable products, insertion of writing of Govt MRP is allowed as per provision laid down in the order of the Central Excise dept. However, for imported item(s), MRP and Trade name may be allowed in addition to Generic name.

  • Description of Facility Provide the following information for all units at the Facility, regardless of their RMR designation status. Information regarding units not designated as Reliability Must-Run Units is required only if and to the extent that the information is used to allocate Facility costs between Reliability Must-Run Units and other units. Unit RMR (Y/N) Maximum Net Dependable Capacity (includes CAISO-paid Upgrade capacity)* Fuel Type For this Facility, the Owner will use [insert either MW, MWhs, or service hours] in Schedule B to allocate Annual Fixed Revenue Requirements to and among Units. This election shall be applicable to all Facilities containing Reliability Must Run Units subject to any “RMR contract” as defined in the CAISO Tariff executed by Owner or any of its affiliates as defined in 18 CFR § 161.2. * Maximum Net Dependable Capacity shall reflect any transformer or line loss to the Delivery Point.

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  • Description of the Project THIS SHOULD BE NO MORE THAN A TWO PARAGRAPH DESCRIPTION THAT PROVIDES A BACKGROUND OF THE PROBLEM, AS WELL AS HOW THE CONTRACTOR INTENDS TO SOLVE THE PROBLEM. KEEP IN MIND THAT THE CONTRACT SHOULD “STAND ON ITS OWN,” I.E. ANYONE SHOULD BE ABLE TO PICK IT UP AND FIGURE OUT WHAT IS GOING ON.)

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