Sensitivity Sample Clauses
The Sensitivity clause defines how information classified as sensitive is to be handled within the context of the agreement. It typically outlines the types of information considered sensitive, such as trade secrets, personal data, or proprietary business details, and sets forth the obligations of the parties to protect this information from unauthorized disclosure or misuse. By establishing clear guidelines for the treatment of sensitive information, this clause helps prevent accidental leaks and ensures compliance with privacy or confidentiality requirements.
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Sensitivity. General Business Use. This Pagdoecu1m2enotfc1on2t1ains proprietary information and is intended for business use only. Date Accepted / / Accepted by ▇▇▇ Accepted by Employer
Sensitivity. The sensitivity of the method is determined by the ability to measure the endogenous CO2 produc- tion of the inoculum in the blank flask and by the sensitivity limit of the dis- solved organic carbon analysis. If the test is adapted to handle 14C-labeled test substances, test substance con- centrations can be much lower.
Sensitivity. All data is considered confidential but not personal sensitive.
Sensitivity. Master data are not considered personal sensitive. All other Data are considered personal sensitive.
Sensitivity. Personal data of the users are considered less sensitive. The content of approval Data, PDF-files and attachments are considered potentially personal sensitive, but beyond the control or influence of Continia.
Sensitivity. Better than *** pV per meter, at minimum
Sensitivity. Participation identifier refers to the company registered is considered less sensitive. The content of XML files can potentially be personal sensitive but beyond the control or influence of Continia. These data are not accessed in order to reach the intended endpoint.
Sensitivity. At the highest level of confidence (level 5, lesion definitely present), sensitivity for correctly localized malignant lesions on digital chest radiography varied from 18% (95% CI: 10%, 32%) to 49% (95% CI: 36%, 63%) at a specificity of 100% (95% CI: 94%, 100%) to 92% (95% CI: 82%, 97%). The false-positive rates in the control group at this level of con- fidence ranged from 0% (0 of 72) to 13% (9 of 72) for observers D and C, respectively. When lesions rated as probably present (level 4) were taken into ac- count, sensitivity increased to 36% (95% CI: 24%, 50%) for observer D and 73% (59%, 84%) for observer A, with specificities of 99% (95% CI: 50%, 76%) and 82% (95% CI: 71%, 90%), respectively (Table 3). Most lesions that had been rated as definitely present at chest radiography
Sensitivity. General Business Use. This document contains proprietary information and is intended for business use only. LINE DRAF REDLINE DRAFT
Sensitivity. Assay sensitivity on the Smart Cycler platform is affected by many factors, including the quality of template preparation, primer and probe design, and optimization of PCR conditions. Quantitative low copy detection is illustrated with an orthopox assay. Reproducible data is achieved through the Smart Cycler’s robust optical, heating and cooling elements. 1 32 33.2 0.14 0.43 % 2 32 33.2 0.13 0.39 % 3 32 33.3 0.17 0.51 % Total mean (n = 96) 33.2 Total SD (n = 96) 0.16 The Smart Cycler system allows detection over a broad range of target concentration. A linear standard curve can be created from a serial dilution, allowing the determination of an unknown sample concentration.