Examples of Study Sites in a sentence
Public Health Program Brochure and our invitation to Prospective Field Study Sites to develop a partnership with TUC to provide essential program information b.
Guidelines for Public Health Field Study Sites & Preceptors, Field Study Overview & Placement Planning Timeline, and Field Study Preceptor Handbook to ensure that proposed sites and preceptors are aware of the required course learning objectives the Program’s approval criteria for Community Health field study placement sites and preceptors, the placement planning timeline, and the field study responsibilities for students, preceptors, sites, and the Program c.
Students are required to review the Approval Criteria for Placement at Unaffiliated Global Health Field Study Sites and submit an Application for Placement at Unaffiliated Global Health Field Study Sites by specified deadlines.
The Clinical Study Sites further consents to the transfer of its financial disclosure data to Nordic Bioscience country of origin, and to the United States of America (“U.S.”) if the Clinical Study Sites is outside of the U.S., even though data protection may not exist or be as developed in those countries as in the Clinical Study Site’s own country.
Sponsor will have the right to use the results of the Study in any manner deemed appropriate to Sponsor’s business interest and Sponsor and Nordic Bioscience will each have the right to report the names of the Clinical Study Sites as required by law or governmental regulation.
The Clinical Study Sites agrees that, for each listed or identified Clinical Investigator who is directly involved in the treatment or evaluation of research subjects, shall return to Nordic Bioscience a financial disclosure form that has been completed and signed by such Clinical Investigator, which shall disclose any applicable interests held by those investigators or subinvestigators or their spouses or dependent children.
Neither Nordic Bioscience nor Sponsor will be responsible for any adverse reactions, which are the result of the negligence or misconduct of the Clinical Study Sites, Principal Investigators or any of their representatives.
This analysis and consultation shall be documented in an exemption notice.
The Clinical Study Sites and Principal Investigators shall permit Nordic Bioscience and agencies such as the FDA to inspect Study records including the Subjects’ medical records.
Clinical Study Sites shall notify Nordic Bioscience immediately upon any inquiry concerning, or the commencement of any such proceeding concerning Clinical Study Sites, Principal Investigators or any such agent or employee.