Primary language means the dominant language used by a person for communication.
plain language means language that can be understood by a reasonable person, applying a reasonable effort;
Speech-language pathology means the care and services provided by a licensed speech-language pathologist as set forth in the member state's statutes and rules.
Speech-language pathologist means an individual who is licensed by a state to practice speech-language pathology.
Native language means, if used in reference to an individual of limited English proficiency, the following:
English language learner means limited English proficient pupils who speak a language other than English as their primary language and have difficulty speaking, reading, writing, or understanding English as reported to the center.
English Language French Language:
Protocol means, in respect of any category of object and associated rights to which this Convention applies, the Protocol in respect of that category of object and associated rights;
Version of a variant means vehicles, which consist of a combination of items shown in the information package subject to the requirements in Annex VIII.
Approved laboratory means a laboratory that is listed in the national conference of interstate milk shipments list of sanitation compliance and enforcement ratings distributed by the United States food and drug administration and as approved by the director.
Unproven/ Experimental treatment means the treatment including drug experimental therapy which is not based on established medical practice in India.
Study means the investigation to be conducted in accordance with the Protocol.
Clinical Study means a Phase I Study, Phase II Study, Phase III Study, as applicable.
Market Analysis means a technique used to identify market characteristics for specific goods or services “National Treasury” has the meaning assigned to it in section 1 of the Municipal Finance Management Act, 2003 (Act No. 56 of 2003);
Clinical laboratory means a facility for the microbiological, serological, chemical, hematological, radiobioassay, cytological, immunohematological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of a disease or assessment of a medical condition.
FDA means the United States Food and Drug Administration and any successor agency thereto.
Adverse Drug Experience means any of: an “adverse drug experience,” a “life-threatening adverse drug experience,” a “serious adverse drug experience,” or an “unexpected adverse drug experience,” as those terms are defined at either 21 C.F.R. § 312.32 or 21 C.F.R. § 314.80.
Reference biological product means the single biological product licensed pursuant to 42 U.S.C.
Language means all documents and correspondence in respect of this contract shall be in English Language.
Common Language Location Identifier (CLLI) codes provide a unique 11-character representation of a network interconnection point. The first 8 characters identify the city, state and building location, while the last 3 characters identify the network component.
Technical Proposal means the Contractor’s Technical Proposal dated (Technical Proposal date).
Urgent Works means any urgent measures, which in the opinion of the Engineer-in-charge become necessary during the progress of the work to obviate any risk of accident or failure or which become necessary for security.
Approved clinical trial means a phase I, phase II, phase III, or phase IV clinical trial that is conducted in relation to the prevention, detection, or treatment of cancer or other life-threatening disease or Condition and is described in any of the following:
TO Technical Proposal means the TO Contractor’s technical response to the CATS+ TORFP dated date of TO Technical Proposal.
Campaign means all activities for or against the election of a candidate for elective state office or for or against a state question;
Phase I Clinical Study means a human clinical study of a product, the principal purpose of which is a preliminary determination of safety in healthy individuals or patients, as described in 21 C.F.R. 312.21(a).