Impurities. The broken stone shall be free from dust and dirt and shall be washed as necessary to ensure that all faces of the stones are perfectly clean. The minimum individual percentages by weight of deleterious substance in any size of coarse aggregate shall not exceed the following values: Materials passing through No.100 screen (ASTM) 1% Shale 1% Coal 1% Soft fragments 1% Clay lumps 1% Other deleterious substances 1% The sum of the percentage by weight of all deleterious substances in any size shall not exceed 5%.
Impurities. The coal supplied under this Agreement shall be washed coal, crushed to two inch (2") maximum top size, and shall be substantially free of impurities, such as bone, slate, rock, wood, metal and other mine debris. AND EXCHANGE COMMISSION PURSUANT TO A REQUEST FOR CONFIDENTIAL TREATMENT Exhibit 10.3
Impurities. The material supplied under these specifications shall contain no soluble mineral or organic substances in quantities capable of producing deleterious or injurious effects under public health or water quality.
Impurities. The natural gas must be technically free of dust, iron oxide, sludge, solid bodies, liquid hydrocarbons and must not be odorized.
Impurities. Recognised potential impurities arising from the cell line or during the manufacturing process
Impurities. [**] [**] [**]
Impurities. Water produced and result of the analysis
Impurities. The composition of the LNG loaded at the Delivery Point shall when converted to a gaseous state contain impurities (in milligrams per NCM except as otherwise stated) of not more than: Mercury Xng/NCM Hydrogen Sulphide Xmg/NCM Carbonyl Sulphide plus Xmg/NCM Hydrogen Sulphide Total Sulphur Xmg/NCM Carbon Dioxide X ppm on v volume maximum Oxygen 0 ppm on volume maximum
Impurities. Organichem shall isolate and fully characterize all known or suspected impurities for the API and provide samples of all impurities to Purepac in a timely manner to prevent delay of the submission of the Product ANDAs. For the purposes of this section, all known or suspected impurities shall be defined as those impurities that are determined to be present in accordance with FDA Rules and as specified from time to time in the USP.
Impurities. Notwithstanding the foregoing, ERN will use Commercially Reasonable Efforts to assist Zavante in answering any questions FDA may have with regard to ERN’s information as listed in ANNEX 6. Zavante acknowledges that finalizing the characterization identification and qualification is a complex process for ERN with some uncertainty of result, and that ERN is only obliged to carry out its Commercially Reasonable Efforts during the process, and which, if it fails (for impossibility of achieving a technically acceptable result, or for the impossibility of ERN to act beyond its Commercially Reasonable Efforts), ERN will in no way be responsible for indemnifying Zavante for its investment in clinical studies for FDA approval, or in facilities or other kind of investment, which Zavante undertakes exclusively at its own risk and expense. In no case will ERN perform clinical studies for qualifying a degradation product.