Subinvestigators Sample Clauses

Subinvestigators. Institution will not use any subinvestigator for the Study without AbbVie’s prior written consent, and only upon Institution’s agreement to ensure any subinvestigator’s compliance with the terms and conditions of this Agreement
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Subinvestigators. Principal Investigator will supervise the conduct of the Clinical Trial, and may appoint such other qualified employees of Institution as subinvestigators (“Subinvestigators”), in accordance with Applicable Law and the Protocol, to assist in the conduct of a Clinical Trial and Institution shall ensure that Principal Investigator shall be responsible for leading and supervising any such Subinvestigator or team of Subinvestigators. The jíž byla uložena sankce zákazu výkonu činnosti, či jí nebylo odebráno příslušné oprávnění ze strany FDA na základě zákona “Generic Drug Enforcement Act” z roku 1992 nebo na základě jakéhokoli obdobného regulatorního či zákonného předpisu či navazující legislativy, pravidel či právních předpisů, Instituce a Hlavní zkoušející souhlasí, že neprodleně písemně vyrozumí Společnost a CRO, dozví-li se kterýkoli z těchto subjektů, že jakékoli takové osobě byla uložena sankce zákazu výkonu činnosti či xx xxxx odejmuto příslušné oprávnění, nebo, že bylo zahájeno řízení, jehož výsledkem může být uložení takové sankce či odejmutí oprávnění po dobu provádění Klinického hodnocení či po jeho provedení. 2.5
Subinvestigators. Institution will not use any subinvestigator for the Study without AbbVie’s prior consent, and shall ensure any such subinvestigator’s compliance with the terms and conditions of this Agreement, including, without limitation, the terms regarding Intellectual Property ownership and confidentiality obligations. In addition, as to any such subinvestigator not employed by Institution, Institution will require such subinvestigator to obtain and provide a copy of an acknowledgement by such subinvestigator’s employer that such subinvestigator is participating in the Study and is obligated to comply with the terms and conditions of this Agreement.
Subinvestigators. Principal Investigator will supervise the conduct of the Clinical Trial, and may appoint such other qualified employees of Institution as subinvestigators (“Subinvestigators”), in accordance with Applicable Law and the Protocol, to assist in the conduct of a Clinical Trial and Institution shall ensure that Principal Investigator shall be responsible for leading and supervising any such Subinvestigator or team of Subinvestigators. The Principal Investigator is an employee of Institution and Institution accepts full responsibility for the Principal Investigator’s conduct of the Clinical Trial and compliance with this Agreement and the Protocol, and holds Principal Investigator responsible to Institution to carry out the Clinical Trial in strict accordance with the terms of this Agreement and the Protocol. Institution may not assign the conduct of the Clinical Trial to a different principal investigator without prior written authorization from Company.
Subinvestigators. INSTITUTION hereby agrees that as to any individuals identified on the applicable FDA Form 1572 or Investigator Information and Agreement Form as subinvestigators for a Study, INSTITUTION shall ensure such individuals’ compliance with the terms and conditions hereof and the applicable Statement of Work.

Related to Subinvestigators

  • Investigator Where a difference arises between the parties relating to the dismissal, discipline or suspension of an employee, or to the interpretation, application, operation or alleged violation of this agreement, including any questions as to whether a matter is arbitrable, during the term of the collective agreement, an arbitrator agreed to by the parties shall, at the request of either party: (a) investigate the difference; (b) define the issue in the difference; and (c) make written recommendations to resolve the difference within five days of the date of receipt of the request and for those five days from that date time does not run in respect of the grievance procedure. The parties agree that this procedure will not be invoked until the grievance procedure has been completed.

  • Investigatory Interview When the employee under investigation is to be interviewed concerning the alleged conduct which could result in discharge or other discipline, the employee and his or her representative shall be notified in writing, at least forty-eight (48) hours prior to the interview. In the event of an emergency, such reasonable notice as the circumstances permit shall be given. The notice shall state that an official investigation is being conducted and shall state the subject matter of the investigatory interview. a. Prior to being interviewed pursuant to this section, the employee shall be afforded a reasonable opportunity and facilities to contact and consult privately with his or her union representative or union attorney. b. Any interview of an employee under this section shall be conducted at a reasonable time, at a suitable location and, when practicable, on the department’s premises when the employee is on duty. The union representative or union attorney may participate in the interview. c. The interview shall be limited to questions that are directly, narrowly, and specifically related to the employee’s job performance as it relates to the allegation(s) or complaints. The employee shall not be subjected to any offensive language nor be threatened with transfer, dismissal or other disciplinary action. Confidentiality of the interview shall be maintained.

  • Investigatory Interviews ‌ A. Upon request, an employee has the right to a union representative at an investigatory interview called by the Employer, if the employee reasonably believes discipline could result. An employee may also have a union representative at a pre-disciplinary meeting. If the requested representative is not reasonably available, the employee will select another representative who is available. Employees seeking representation are responsible for contacting their representative.

  • Institution and Investigator acknowledge and agree that its, his or her judgment with respect to its, his or her advice to and care of each Subject is not and shall not be affected by the compensation Institution and/or Investigator receive in accordance with the Study.

  • Principal Investigator The Research will be supervised by __________________ ("Principal Investigator"). If for any reason the individual is unable to continue to serve as Principal Investigator and a successor acceptable to both the University and the Sponsor is not available, this agreement shall be terminated as provided in Article 9. The Principal Investigator may work with others at the University (“Associates”) in conducting the Research.

  • Liaisons Each party shall designate a representative to serve as its liaison in all matters arising under this Agreement, and shall furnish in writing the name of each representative to the other party.

  • 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 xxxx 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.

  • Grievance Investigations Where an employee has asked or is obliged to be represented by the Institute in relation to the presentation of a grievance and an employee acting on behalf of the Institute wishes to discuss the grievance with that employee, the employee and the representative of the employee will, where operational requirements permit, be given reasonable leave with pay for this purpose when the discussion takes place in the headquarters area of such employee and leave without pay when it takes place outside the headquarters area of such employee.

  • Geotechnical Investigation Perform in accordance with the City Design Manual and other City requirements as designated in writing by the Director.

  • Regulatory Investigations TCI and TLIC agree to cooperate fully in any insurance or judicial regulatory investigation or proceeding arising in connection with Contracts distributed under this Agreement. TCI and TLIC further agree to cooperate fully in any securities regulatory inspection, inquiry, investigation or proceeding or any judicial proceeding with respect to TLIC, TCI, their affiliates and their representatives to the extent that such inspection, inquiry, investigation or proceeding or judicial proceeding is in connection with Contracts distributed under this Agreement. Without limiting the foregoing: (a) TCI will be notified promptly of any customer complaint or notice of any regulatory inspection, inquiry investigation or proceeding or judicial proceeding received by TLIC with respect to TCI or any representative or which may affect TLIC’s issuance of any Contracts marketed under this Agreement; and (b) TCI will promptly notify TLIC of any customer complaint or notice of any regulatory inspection, inquiry, investigation or judicial proceeding received by TCI or any representative with respect to TLIC or its affiliates in connection with any Contracts distributed under this Agreement. In the case of a customer complaint, TCI and TLIC will cooperate in investigating such complaint and shall arrive at a mutually satisfactory response.

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