Research Injury Sample Clauses

Research Injury. For purposes of this indemnification and research injury policy, the term “Research Injury” means physical injury caused by treatment or procedures required by the Protocol that the Study subject would not have received if the subject had not participated in the Study. Institution agrees to provide or arrange for prompt diagnosis and medical treatment of any Research Injury experienced by a Study subject. Institution further agrees to promptly notify Sponsor of any Research Injury within thirty (30) days of receiving notice of the Research Injury. 3
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Research Injury. For purposes of this indemnification and subject injury section, the term “Research Injury” means physical injury caused by treatment or procedures required by the Protocol that the Study subject would not have received if the Study participant had not participated in the Study. UNIVERSITY agrees to provide or arrange for prompt diagnosis and treatment of any Research Injury experienced by a Study participant as soon as UNIVERSITY becomes aware of the Research Injury. It is the policy of the UNIVERSITY to provide neither financial compensation nor free treatment for research-related injury. Accordingly, any such treatment will be provided at the usual charge. UNIVERSITY further agrees to promptly notify SPONSOR of any Research Injury upon becoming aware of such injury.
Research Injury. For purposes of this Indemnification and Research Injury Policy, the term “Research Injury” means adverse event, physical injury, or illness caused by treatment or procedures required by the Protocol that the Study Subject would not have received if the Subject had not participated in the Study. Because this is an observational study involving Study Subjects who are receiving prescribed treatment with the Pfizer Product as part of their standard medical care, an adverse reaction to the Pfizer Product would not be a Research Injury. Institution agrees to provide or arrange for prompt diagnosis and medical treatment of any Research Injury experienced by a Study Subject. Institution further agrees to promptly notify CRO of any Research Injury. If any study-specific terms are needed for this Study, add them here. Include identification of any prospectively authorized assignment or delegation by Institution. If an additional term is intended to override an inconsistent provision of the Master Agreement, identify the inconsistent Master Agreement provision and obtain prospective approval to override it from Alliance Partner Legal (AP studies) or Pfizer Legal (CRO studies).
Research Injury 

Related to Research Injury

  • Musculoskeletal Injury Prevention and Control (a) The Hospital in consultation with the Joint Health and Safety Committee (JHSC) shall develop, establish and put into effect, musculoskeletal prevention and control measures, procedures, practices and training for the health and safety of employees.

  • Industrial Injury or Illness 9.1 Any employee who is disabled in the discharge of his/her duties and if such disablement results in absence from his/her regular duties, shall be compensated, except as otherwise hereinafter provided, in the amount of eighty percent (80%) of the employee's normal hourly rate of pay, not to exceed two hundred and sixty-one (261) regularly scheduled workdays counted from the first regularly scheduled workday after the day of the on-the-job injury; provided the disability sustained must qualify the employee for benefits under State Industrial Insurance and Medical Aid Acts.

  • Services to Treat an Accidental Injury This plan covers the following services to treat an accidental injury to your sound natural teeth or an injury resulting in a facial fracture, received in an emergency room or provider’s office when the treatment is received within seventy-two (72) hours of the injury. • Extraction of teeth needed to avoid infection of teeth damaged in the injury; • Suturing; • Reimplanting and stabilization of dislodged teeth; • Repositioning and stabilization of partly dislodged teeth; and • Dental x-rays.

  • Industrial Injury Leave Employees suffering an industrial injury shall be granted leave in accordance with the applicable state and federal law. Employees returning from such leave of absence shall be reinstated to that individual's former position or one of like status and pay without loss of seniority or accrued benefits. This paragraph shall in no way restrict the Employer from disciplining employees up to and including termination for violation of Employer's written safety procedures or policies.

  • High Risk Use Npcap is not designed, manufactured, or intended for use in hazardous environments requiring fail-safe performance where the failure of the software could lead directly to death, personal injury, or significant physical or environmental damage (“High Risk Activities”). Use of Npcap in High Risk Activities is not authorized.

  • DEVELOPMENT OR ASSISTANCE IN DEVELOPMENT OF SPECIFICATIONS REQUIREMENTS/ STATEMENTS OF WORK Firms and/or individuals that assisted in the development or drafting of the specifications, requirements, statements of work, or solicitation documents contained herein are excluded from competing for this solicitation. This shall not be applicable to firms and/or individuals providing responses to a publicly posted Request for Information (RFI) associated with a solicitation.

  • Insurance, Subcontractor's Public Liability and Property Damage The Contractor shall require each of its subcontractors to secure and maintain during the life of the subcontract, insurance of the type specified in this Contract, or, the Contractor may insure the activities of its subcontractors in the Contractor’s policy, as specified in this Contract.

  • Research Use The Requester agrees that if access is approved, (1) the PI named in the DAR and (2) those named in the “Senior/Key Person Profile” section of the DAR, including the Information Technology Director and any trainee, employee, or contractor1 working on the proposed research project under the direct oversight of these individuals, shall become Approved Users of the requested dataset(s). Research use will occur solely in connection with the approved research project described in the DAR, which includes a 1-2 paragraph description of the proposed research (i.e., a Research Use Statement). Investigators interested in using Cloud Computing for data storage and analysis must request permission to use Cloud Computing in the DAR and identify the Cloud Service Provider (CSP) or providers and/or Private Cloud System (PCS) that they propose to use. They must also submit a Cloud Computing Use Statement as part of the DAR that describes the type of service and how it will be used to carry out the proposed research as described in the Research Use Statement. If the Approved Users plan to collaborate with investigators outside the Requester, the investigators at each external site must submit an independent DAR using the same project title and Research Use Statement, and if using the cloud, Cloud Computing Use Statement. New uses of these data outside those described in the DAR will require submission of a new DAR; modifications to the research project will require submission of an amendment to this application (e.g., adding or deleting Requester Collaborators from the Requester, adding datasets to an approved project). Access to the requested dataset(s) is granted for a period of one (1) year, with the option to renew access or close-out a project at the end of that year. Submitting Investigator(s), or their collaborators, who provided the data or samples used to generate controlled-access datasets subject to the NIH GDS Policy and who have Institutional Review Board (IRB) approval and who meet any other study specific terms of access, are exempt from the limitation on the scope of the research use as defined in the DAR.

  • High Risk Activities 1. The Software is not fault-tolerant and is not designed, manufactured or intended for use or resale as on-line control equipment in hazardous environments requiring fail-safe performance, such as in the operation of nuclear facilities, aircraft navigation or communication systems, air traffic control, direct life support machines, or weapons systems, in which the failure of the Software could lead directly to death, personal injury, or severe physical or environmental damage ("High Risk Activities"). Syncro and its suppliers specifically disclaim any express or implied warranty of fitness for High Risk Activities.

  • Research Support opioid abatement research that may include, but is not limited to, the following:

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