Conducting Research Clause Samples

The "Conducting Research" clause defines the rules and permissions governing how research activities may be carried out under an agreement. It typically outlines the scope of permissible research, any required approvals or ethical considerations, and the responsibilities of the parties involved, such as data handling or reporting obligations. By establishing clear guidelines for conducting research, this clause helps ensure compliance with legal, ethical, and contractual standards, thereby minimizing misunderstandings and potential disputes.
Conducting Research. Conducting research according to the protocol approved by CPHS. The relying investigators should not implement any revisions or changes to the protocol without prior approval from CPHS, except where necessary to eliminate immediate hazard(s) to research subjects. Necessary changes to the research should be communicated to the reviewing PI. The reviewing PI is responsible for handling the IRB amendment submission to the reviewing IRB.
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Conducting Research. NU shall conduct the Funded Research at its own responsibility and hold Company harmless in relation to the same; provided, however, that Company shall indemnify NU for NU’s losses due to defects in the materials furnished by Company to NU. NU shall provide Company with advanced written notice when a new person at NU participates in the Funded Research as the Researcher.
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Conducting Research. GCRMC complies with federal and state laws and regulations in any research, investigation and clinical trial conducted by our physicians and professional staff. Any human subject research conducted at GCRMC must be consistent with GCRMC policies. Any questions should be referred to GCRMC’s Compliance Officer.
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Conducting Research. The UIW Investigator(s) will conduct research according to the approved protocol and ensure that the planned research activities are approved by the reviewing IRB prior to implementation. The UIW Investigator(s) should not implement any revisions or changes to the protocol without prior approval from the Reviewing IRB, except where necessary to eliminate immediate hazard(s) to research subjects. Necessary changes should be reported to the Non-Affiliated Investigator of the Reviewing IRB. The Non-Affiliated Investigator is responsible for handling the IRB amendment submission to the Reviewing IRB.
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Conducting Research. The Non-affiliated Investigator(s) will conduct research according to the protocol approved by UIW IRB. The Non-affiliated Investigator(s) should not implement any revisions or changes to the protocol without prior approval from the UIW IRB, except where necessary to eliminate immediate hazard(s) to research subjects. Necessary changes to the research should be communicated to the UIW Investigator(s). The UIW Investigator(s) is responsible for handling the IRB amendment submission to the UIW IRB.
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Conducting Research. Research activities, including economic research on the use and impact of IFRS Standards, may be undertaken from time to time.
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Conducting Research. (a) Approval or consent from research participants or hosting organizations shall be gained, unless (b) below holds true. (b) Approval or consent from research participants or hosting organizations is not required only in special cases, such as research with anonymous questionnaires or naturalistic observations. (c) Participants will be informed about the research and its anticipated use(s), in language that is understandable to the general public. (d) Where applicable, research participants shall be suitably protected from adverse consequences of participating in the research, including (but not limited to) potential consequences of withdrawing from the research. (e) If inducements are offered to research participants, such inducements shall not be excessive or inappropriate.
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Conducting Research. Each of the 12 students became a member of two or three study groups, for a total of 1G groups representing the 1G cities participating in the AVIAMA General Assembly. The students started research on puppet theaters in each city. English sources on the Internet 5 Japanese sources on the Internet 8 Visiting organizations 4 Japanese sources at the library 3 English sources at the library 1 Others (Interviewing on the phone) 1 According to the questionnaire, all respondents (N= 5) answered that they read English sources on the Internet (Table 2). To conduct research and gain the necessary information to make a presentation, the students had to purposefully read many English sources. Depending on the students’ needs, the teacher provided information, such as cultural organizations from each country which the students could visit, and references including websites and books they could refer to.
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Related to Conducting Research

  • Research Primary Investigator as part of a multi-site study (25 points) • Co-Investigator as part of a multi-site study (20 points) • Primary Investigator of a facility/unit based research study (15 points) • Co-Investigator of a facility/unit based research study (10 points) • Develops a unit specific research proposal (5 points) • Conducts a literature review as part of a research study (5 points)

  • Development Activities The Development activities referred to in item “b” of paragraph 3.1 include: studies and projects of implementation of the Production facilities; drilling and completion of the Producing and injection ▇▇▇▇▇; and installation of equipment and vessels for extraction, collection, Treatment, storage, and transfer of Oil and Gas. The installation referred to in item “c” includes, but is not limited to, offshore platforms, pipelines, Oil and Gas Treatment plants, equipment and facilities for measurement of the inspected Production, wellhead equipment, production pipes, flow lines, tanks, and other facilities exclusively intended for extraction, as well as oil and gas pipelines for Production Outflow and their respective compressor and pumping stations.

  • 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.

  • Clinical 1.1 Provides comprehensive evidence based nursing care and individual case management to a specific group of patients/clients including assessment, intervention and evaluation. 1.2 Undertakes clinical shifts at the direction of senior staff and the Nursing Director including participation on the on-call/after-hours/weekend roster if required. 1.3 Responsible and accountable for patient safety and quality of care through planning, coordinating, performing, facilitating, and evaluating the delivery of patient care relating to a particular group of patients, clients or staff in the practice setting. 1.4 Monitors, reviews and reports upon the standard of nursing practice to ensure that colleagues are working within the scope of nursing practice, following appropriate clinical pathways, policies, procedures and adopting a risk management approach in patient care delivery. 1.5 Participates in ▇▇▇▇ rounds/case conferences as appropriate. 1.6 Educates patients/carers in post discharge management and organises discharge summaries/referrals to other services, as appropriate. 1.7 Supports and liaises with patients, carers, colleagues, medical, nursing, allied health, support staff, external agencies and the private sector to provide coordinated multidisciplinary care. 1.8 Completes clinical documentation and undertakes other administrative/management tasks as required. 1.9 Participates in departmental and other meetings as required to meet organisational and service objectives. 1.10 Develops and seeks to implement change utilising expert clinical knowledge through research and evidence based best practice. 1.11 Monitors and maintains availability of consumable stock. 1.12 Complies with and demonstrates a positive commitment to Regulations, Acts and Policies relevant to nursing including the Code of Ethics for Nurses in Australia, the Code of Conduct for Nurses in Australia, the National Competency Standards for the Registered Nurse and the Poisons Act 2014 and Medicines and Poisons Regulations 2016. 1.13 Promotes and participates in team building and decision making. 1.14 Responsible for the clinical supervision of nurses at Level 1 and/or Enrolled Nurses/ Assistants in Nursing under their supervision.

  • Development Program A. Development activities to be undertaken (Please break activities into subunits with the date of completion of major milestones) B. Estimated total development time