Research Subject Sample Clauses

Research Subject. A person, family, household, or organization observed for purposes of research and to whom a promise of confidentiality has been given. A Research Subject includes any person providing information to a study or on whose behalf a proxy provides information.
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Research Subject. In this research the researcher used purposive sampling technique. According to (Xxxxxxxx, 2002, p.27), purposive sampling technique is a sampling technique which is done because limited time and finding. According to (Xxxxxxxxxx and xx.xx, 2006, p.140) purposive sampling technique is a common procedure used in qualitative research that identifies key informants or person who have specific knowledge about the topic being studied. The type of purposive sampling that a researcher may decide to use depends on the purpose of the study. it means in this research, researcher xxxx chose the subject according to the need and purpose of the research. Then, the researcher choosed the students at eight grade (class A) by consideration the result of grand tour which revealed they are more active than other classes and they had rule for using English so this class have higher scores in English subjects than other classes. Several students of class A were active to participate the English competition such as role-play, speech contest, story telling and competition of intellegence in English, and the others. Then, the researcher will know students‟ attitude towards English speaking at eight grade (class A) at MTS An-nur Tangkit Islamic Boarding school. The students‟ total in this class were 26 students observed, then 16 students who have been interviewed to know students‟ attitudes toward speaking English more specific. The criteria of selecting participants for this research the active students. It is take from the result grandtour. To protect research ethics, researcher not use the real name of some participants.
Research Subject. The research subject is a source that can provide information on the problem researched by the author. (1). Supervisor, from the two Vocational High Schools studied; (2). Principal, (3). Vice Mayor Xxxxx, (4). Head of study program or head of competency and teachers, (5). Business world and industrial world. To obtain data, 3 techniques were used, namely:

Related to Research Subject

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  • Research Project 48.01 The findings of any research project, which would change the provisions of this Agreement will not be implemented until such changes are negotiated and agreed to by the parties.

  • Clinical Trials The studies, tests and preclinical and clinical trials conducted by or on behalf of, or sponsored by, the Company, or in which the Company has participated, that are described in the Registration Statement, the Time of Sale Disclosure Package or the Prospectus, or the results of which are referred to in the Registration Statement, the Time of Sale Disclosure Package or the Prospectus, were and, if still pending, are being conducted in all material respects in accordance with protocols, procedures and controls pursuant to, where applicable, accepted professional and scientific standards for products or product candidates comparable to those being developed by the Company and all applicable statutes, rules and regulations of the FDA, the EMEA, Health Canada and other comparable drug and medical device (including diagnostic product) regulatory agencies outside of the United States to which they are subject; the descriptions of the results of such studies, tests and trials contained in the Registration Statement, the Time of Sale Disclosure Package or the Prospectus do not contain any misstatement of a material fact or omit a material fact necessary to make such statements not misleading; the Company has no knowledge of any studies, tests or trials not described in the Disclosure Package and the Prospectus the results of which reasonably call into question in any material respect the results of the studies, tests and trials described in the Registration Statement, the Time of Sale Disclosure Package or Prospectus; and the Company has not received any notices or other correspondence from the FDA, EMEA, Health Canada or any other foreign, state or local governmental body exercising comparable authority or any Institutional Review Board or comparable authority requiring or threatening the termination, suspension or material modification of any studies, tests or preclinical or clinical trials conducted by or on behalf of, or sponsored by, the Company or in which the Company has participated, and, to the Company’s knowledge, there are no reasonable grounds for the same. Except as disclosed in the Registration Statement, the Time of Sale Disclosure Package and the Prospectus, there has not been any violation of law or regulation by the Company in its respective product development efforts, submissions or reports to any regulatory authority that could reasonably be expected to require investigation, corrective action or enforcement action.

  • Development Phase contractual phase initiated with the approval of ANP for the Development Plan and which is extended during the Production Phase while investments in xxxxx, equipment, and facilities for the Production of Oil and Gas according to the Best Practices of the Oil Industry are required.

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  • Development Plans 4.3.1 For each Licensed Indication and corresponding Licensed Product in the Field, Licensee will prepare and deliver to Licensor a development plan and budget (each a “Development Plan”). The initial Development Plans for each Licensed Indication will be delivered within […***…] after the Grant Date for such Licensed Indication.

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