Sample Data definition

Sample Data means any data (including from third-party sources) provided or made available to Customer by Snowflake solely for Customer’s internal testing, evaluation, and other non-productive use of the Service during the Subscription Term.

Sample Data is defined in Section 5.3(a).

Sample Data means any sample data that may be provided by Cloudera for use with Free Trial Services, including without limitation, in a Cloudera Sample VPC.

Examples of Sample Data in a sentence

• The concentration of pollutant (an arithmetic mean or a median) in these samples estimated from the “Multiple Sample Data Reduction” section above, will be used for compliance determination.In the event of noncompliance with an AMEL, the sampling frequency for that parameter shall be increased to weekly and shall continue at this level until compliance with the AMEL has been demonstrated.

• Permittees may be considered out of compliance with the effluent limitation if the concentration of the pollutant (see section B “Multiple Sample Data Reduction” above) in the monitoring sample is greater than the effluent limitation and greater than or equal to the RL.

• U.S. Census Bureau, Census 2000, Summary File 3 (SF 3) Sample Data.

• Agreed-Upon Procedures’ FindingsThe results of the foregoing procedures indicated that the Characteristics as set forth on the Sample Data File were found to be in agreement with the Loan Documents, except for those items listed on the attached Appendix A.

• The CSF Inventory Sheet is used to record both the inventory of CSF documents and the number of documents in the original Sample Data Package which is sent to the EPA Region.

More Definitions of Sample Data

Sample Data means all data (including raw data), findings, conclusions and other results from the Sample Analyses.

Sample Data shall have the meaning set forth in Article 11.2 b. „Data o vzorku“ má stejný význam jako v článku 11.2 b.

Sample Data means any pre-populated data provided in the Trial Services to enable Customer to use the Trial Services without entering its own Customer Data; “Intellectual Property Rights” means unpatented inventions, patent applications, patents, design rights, copyrights, trademarks, service marks, trade names, domain name rights, mask work rights, know-how and other trade secret rights, and all other intellectual property rights, derivatives thereof, and forms of protection of a similar nature anywhere in the world; “Order Form(s)” means the form evidencing the initial subscription order for the Services and any subsequent Order Forms submitted online or in written form, specifying, among other things, the Services contracted for, the applicable Fees, the billing period, and other charges as agreed to between the parties; “Gamma Technology”means all of Gamma’s proprietary technology (including Sample Data, software, hardware, products, processes, algorithms, user interfaces, know-how, techniques, designs and other tangible or intangible technical material or information) made available to Customer by Gamma in providing the Trial Services; “Service(s)” means Gamma’s data flow monitoring, data access controls, data transformation and redaction services to which Customer is being granted access to on a trial basis under this Agreement, including the Gamma Technology, the

Sample Data means any information that does not personally identify any individual, drawn or deduced from analysis of a Sample by or for Ombre.

Sample Data means data in, originating from, or derived from an information system consumable form that mimics or is representative of real-world operational data which may be used for testing, demonstrations or other purposes and that is made available to Ordering Activity under this Agreement.

Sample Data shall have the meaning set forth in Section 13.2. 1.19 “Sponsor Drug” shall mean the Sponsor’s product that is being studied in the Trial. If the Sponsor’s product is being studied in the Trial in combination with another product, “Sponsor Drug” shall mean the combination. 1.20 “Sponsor Indemnitees” shall have the meaning set forth in Section 0 . 1.21 “Trial” shall mean the multi-center clinical trial to be performed in accordance with the Protocol. kombinácii s R-CHOP v porovnaní s R-CHOP samostatne u predtým neliečených stredne- vysoko a vysoko rizikových pacientov s novo diagnostikovaným difúznym veľkobunečným B- lymfómom (DLBCL)“ a každý protokol spoločnosti, ktorý neskôr písomne vypracuje a schváli Zadávateľ a podpíše HS, a ktorý sa realizuje súbežne so všetkými alebo rovnakými Subjektmi Skúšania, vrátane všetkých dodatkov vyššie uvedených dokumentov. Aby sa predišlo pochybnostiam, Protokol sa pokladá za finálny dokument po jeho podpise Zadávateľom a HS a schválení príslušnou nezávislou EK. Potom sa môžu dodatky k Protokolu vypracovať len pod vedením Zadávateľa a po následnom schválení nezávislej EK. 1.15 „Záznamy” znamenajú Záznamy skúšania o Subjektoch skúšania, čo zahŕňa kópie všetkých Údajov skúšania Inštitúcie a HS, ako aj všetky súvisiace zdrojové dokumenty. 1.16 „Zástupca” má význam, aký sa uvádza v Článku 24.2. 1.17 „Údaje výskumu” majú význam, aký sa uvádza v Článku 10.4. 1.18 „Údaje o vzorkách” majú význam, aký sa uvádza v Článku 13.3. 1.19 „Produkt Zadávateľa“ znamená produkt Zadávateľa, ktorý sa v Skúšaní skúma. Ak sa Produkt Zadávateľa skúma v Skúšaní v kombinácii s iným produktom, „Produkt zadávateľa“ znamená ich kombináciu. 1.20 „Odškodnené osoby Zadávateľa” majú význam, aký sa uvádza v Článku 19.1. 1.21 „Skúšanie” znamená multicentrické klinické skúšanie, ktoré sa má realizovať v súlade s Protokolom.

Sample Data shall have the meaning set forth in Section 13.2.