Subinvestigators Sample Clauses

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
Sample 1
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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.
Sample 1
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
Sample 1
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.
Sample 1
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.
Sample 1

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:

  • 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.

  • Investigatory Interviews When an employee is required by the City to attend an interview conducted by the City for purposes of investigating an incident which may lead to discipline/discharge of that employee because of that particular incident, the employee shall have the right to request that the employee be accompanied at the investigatory interview by a representative of the Union. If the employee makes such a request, the request shall be made to the City representative conducting the investigatory interview. The City, when faced with such a request, may:

  • Institution and Investigator acknowledge that SPONSOR has no obligation to indemnify or be responsible for any loss, claim, cost (including reasonable attorney fees) or demand if and to the extent such losses, claims or demands arise from any injuries or damages resulting from Institution’s, Investigator’s or the Study Personnel’s negligence, breach of this Agreement, failure to adhere to the Protocol, failure to obtain signed informed consent forms, failure to follow Applicable Law, misuse of the Study Drug, unauthorized warranties, or willful misconduct. This indemnification obligation is without prejudice to the precedence of insurance coverage from compulsory clinical trial insurance. 12.3. Zdravotnické zařízení a zkoušející berou na vědomí, že ZADAVATEL nevyplatí žádné odškodnění ani není odpovědný za žádné ztráty, náklady, spory (včetně přiměřených nákladů na právní pomoc) či nároky v souvislosti s újmou či škodou, ke kterým došlo v důsledku nedbalosti na straně zdravotnického zařízení, zkoušejícího a/nebo členů týmu provádějícího klinické hodnocení a/nebo v důsledku toho, že zdravotnické zařízení, zkoušející a/nebo některý člen týmu provádějícího klinické hodnocení porušili ustanovení této smlouvy, porušili ustanovení protokolu, nenechali subjekt hodnocení podepsat informovaný souhlas, porušili ustanovení platných zákonů, chybným způsobem použili studijní léčivo ZADAVATELe, způsobili škodu úmyslným zaviněním a/nebo poskytli neoprávněné záruky. Touto povinností odškodnění není dotčeno přednostní pojistné krytí z povinného pojištění klinického hodnocení.

  • Principal Investigator The research will be under the direction of (“Principal Investigator”). If, for any reason, he/she is unable to continue to serve as Principal Investigator and a successor acceptable to both UHD and Sponsor is not available, this Agreement shall be terminated as provided in Section 7.

  • Investigatory Meetings A. An employee required to attend an investigatory meeting shall receive advance notice of such meeting. Such notice shall include:

  • Project Team Cooperation Partnering 1.1.3 Constitutional Principles Applicable to State Public Works Projects.

  • 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.

  • PROFESSORS, TEACHERS AND RESEARCHERS 1. An individual who is a resident of a Contracting State immediately before making a visit to the other Contracting State, and who, at the invitation of any university, college, school or other similar educational institution which is recognized by the competent authority in that other Contracting State, visits that other Contracting State for a period not exceeding two years solely for the purpose of teaching or research or both at such educational institution shall be exempt from tax in that other Contracting State on any remuneration for such teaching or research.

  • Clinical 2.1 Provides comprehensive evidence based nursing care to patients including assessment, intervention and evaluation.

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