Clinical Hours Sample Clauses

Clinical Hours. This section addresses the load for instruction of students who are participating in work-based learning activities that are part of the student’s program of study. These activities may be variously entitled clinical affiliations, internships, externships, or practicums – but within this article all similar activities shall be referenced as clinicals. For these activities, the load shall be calculated as follows:
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Clinical Hours. Bargaining unit members may use their scheduled planning time to complete professional clinical hours to fulfill the requirements of their educational programs. In completing these hours:
Clinical Hours. In addition to the event and practice coverage set forth in Section 2(a) above, MNPG will provide up to eight (8) hours per week of clinical athletic training services to the school during the term of the Agreement. Specific times and locations for the clinical services shall be determined and agreed upon by the parties hereto.
Clinical Hours. Full-time NP/PAs shall have thirty-two (32) scheduled clinical hours per week, except for those NP/PAs working in Urgent Care who will have thirty-four (34) scheduled clinical hours per week. Within sixty (60) days following ratification, the Parties will establish a committee that will meet and confer in regards to ensuring that the proposed additional clinical hours are clearly defined.

Related to Clinical Hours

  • 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.

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  • Laboratory Testing All laboratories selected by UPS Freight for analyzing Controlled Substances Testing will be HHS certified.

  • Biological Samples If so specified in the Protocol, Institution and Principal Investigator may collect and provide to Sponsor or its designee Biological Samples (“Biological Samples”). 12.2.

  • Trials The Ship shall run the following test and trials:

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