Institutional Official definition

Institutional Official means the legal representative of Institution who is authorized to enter into legally binding agreements on behalf of Institution.

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Institutional Official means one or more persons designated by the College as having responsibilities and authority under this Policy.

Institutional Official means an employee of Umpqua Community College when acting in the course and scope of their employment duties.

Examples of Institutional Official in a sentence

• If the Residency Program Director does not reconcile or cure the alleged inconsistency, it shall be the obligation of Resident to notify the institution’s Designated Institutional Official (“DIO”) who shall take the necessary steps to reconcile or cure any actual inconsistency.

• DIO – Designated Institutional Official – A liaison to the Accreditation Council for Graduate Medical Education.

• Provide the Institutional Official of the engaged institution with information about the IRB, such as a list of IRB members or expertise and the written procedures for executing IRB responsibilities in accordance with paragraph A.8 above.

• Accordingly, Resident shall neither accept nor engage in employment outside of the Program, (moonlighting) either in SRHS facilities or with outside healthcare facilities without the prior written approval of the Resident’s Program Director and the Designated Institutional Official.

• To notify the Program Director and the Designated Institutional Official immediately if any license cited above expires without renewal or is suspended, revoked or limited in any manner, or if any action by any licensing authority, court or government agency regarding licensure, controlled substance authorization, criminal activity initiates an investigation or disciplinary proceedings against the Resident.

More Definitions of Institutional Official

Institutional Official. (IO) means the individual responsible for implementation of this Regulation and associated SOPs and is the institution’s Chief Research Officer. The IO delegates this authority to the COIO, but remains ultimately responsible.

Institutional Official means the individual within the Institution with authority and oversight for the solicitation and review of disclosures of Significant Financial Interests including those of the Investigator’s Family related to the Investigator’s Institutional Responsibilities. For the purposes of this Regulation, the Institutional Official is designated as the Vice Chancellor for Research and Graduate Studies. Implementation is delegated to the COIO, Assistant Director of the Office of Research Integrity and Compliance (ORIC).

Institutional Official means the individual, within the Institution and designated by the Institution, who is responsible for the solicitation and review of disclosures of Significant Financial Interests of each Investigator that is planning to participate in, or is participating in, any PHS-funded Research, including pursuant to any subaward under the prime award from the PHS Grantee, including those of the Investigator’s Family. For the purposes of this policy, the initial Institutional Official designated by the Institution shall be Dipl.-Betrw. Thomas Forstmann, who works at the Institution. The Institution (or FhG acting on behalf of the Institution) may replace the Institutional Official at its convenience, in which case such replacement official shall act as the Institutional Official for purposes of this policy.

Institutional Official means the UNT Vice President for Research and Innovation, as appointed by the University President, has the authority to sign the UNT Assurance, making a commitment on behalf of UNT that the requirements of the PHS Policy will be met.

Institutional Official means the person appointed by the Provost (or his or her designee) to serve in such position.

Institutional Official is the legal representative of the Institution receiving the NEI-AREDS2 Repository Samples (“Institution”) who is authorized to make legally binding agreements for the Institution (see Appendix 1). The Principal Investigator (“Recipient”) is the person receiving the NEI Repository Sample(s) and is responsible for the conduct of the Statement of Research Intent, defined below. The Recipient’s research team that is under the direct supervision of the Recipient may have access to the NEI Repository Sample(s) only after they have been informed of and agreed to the provisions of this MTA. The Recipient must acknowledge on the signature page of this MTA that the Recipient has read and understands the terms and conditions of this MTA. The Institutional Official must also sign this MTA on behalf of the Institution agreeing to adhere to the terms and conditions of this MTA. To ensure compliance with the Office for Human Research Protections (“OHRP”), Department of Health and Human Services (“DHHS”), regulations for the protection of human subjects (45 CFR Part 46), before NEI-AREDS2 Repository Samples can be shipped from the Repository, the Recipient must provide the Repository with a written description of the purpose of the research project to be done using the applicable NEI-AREDS2 Repository Samples (“Statement of Research Intent”) and this MTA. Both the Recipient and the Institutional Official must sign this MTA agreeing to adhere to the conditions set forth in this MTA. The Recipient remains subject to all applicable local, state, and federal laws and regulations and Institution policies. The signed Statement of Research Intent and MTA must be returned to ▇▇▇▇▇▇▇ prior to ▇▇▇▇▇▇▇ shipping the applicable NEI-AREDS2 Repository Samples.

Institutional Official. The Institutional Official is the Signatory Official on each Institution’s FWA filed with OHRP to assure compliance with regulations governing protection of human subjects. OHRP requires the Institution Official to be a high-level official who has the authority to represent the Institution named in the FWA.  Reportable Events – Any event, including adverse event, unanticipated problems, protocol violations, noncompliance with applicable laws and regulations, incidents, concerns, injuries to subjects related to a protocol intervention, and/or complaints that are required to be reported to the Reviewing IRB in accordance with its policies and guidelines.