Diagnostic study definition

Diagnostic study means a laboratory test, X-ray, ultrasound, or procedure used to identify a characteristic or distinguishing feature of a particular disease or condition.
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Diagnostic study means a laboratory test, X-ray, ultrasound, or other procedure used
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Diagnostic study means a study of a highway railroad grade crossing and any adjacent factors that will have an impact upon the operation at the grade crossing. This study shall be initiated by the department rail manager and shall be conducted by a diagnostic team constituted by the rail manager. Any reports submitted shall be stamped and signed by a registered engineer licensed in the state of New Mexico. A diagnostic study of a crossing shall be based on criteria and standards identified in the reference documents in subsection B of 18.14.4.8 NMAC.
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Examples of Diagnostic study in a sentence

  • Shall perform the following procedures: Process Procedure Preparatory - Diagnostic study models - Models, mounting, duplicating - Polishing 1ST 6 months 13.20 Thereafter* 15.53 Asst II training for Asst I 1ST 6 months 15.53 2nd 6 months * 16.15 Thereafter* 16.49 13.53 15.92 15.92 16.55 16.90 13.90 16.36 16.36 17.01 17.37 Orthodontics Technician Assistant I..............................................


More Definitions of Diagnostic study

Diagnostic study means any test used to help establish or exclude the presence of disease/injury in symptomatic persons. The test may help determine the diagnosis, screen for specific disease/injury, guide the management of an established disease/injury, and formulate a prognosis.
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Diagnostic study means a laboratory test, X-ray, ultrasound, or procedure
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Diagnostic study means a laboratory test, X-ray, ultrasound, or procedure used to
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Related to Diagnostic study

  • Diagnostic Product means an assemblage of reagents, including but not limited to reagents packaged in the form of a kit, useful in performing a Licensed Service.

  • Clinical Study means a Phase I Study, Phase II Study, Phase III Study, as applicable.

  • Phase I Trial means a clinical trial of a Licensed Product in human patients designated as a Phase I Trial and conducted primarily for the purpose of determining the safety of and/or the metabolism and pharmacologic actions of the Licensed Product in humans, as described under 21 CFR § 312.21(a) (as hereafter modified or amended) and any of its foreign equivalents. For purposes of this definition, Phase I Trial shall specifically exclude trials in healthy volunteers.

  • Phase III Trial means a Clinical Trial of an investigational product in subjects that incorporates accepted endpoints for confirmation of statistical significance of efficacy and safety with the aim to generate data and results that can be submitted to obtain Regulatory Approval as described in 21 C.F.R. 312.21(c), or a comparable Clinical Trial prescribed by the relevant Regulatory Authority in a country other than the United States.

  • Phase I Study means a human clinical trial in any country that would satisfy the requirements of 21 C.F.R. § 312.21(a) (FDCA), as amended from time to time, and the foreign equivalent thereof.