Performance of the Clinical Sample Clauses

Performance of the Clinical. Trial 1.1 The parties agree that the Protocol, including any subsequent Protocol amendments, if not attached hereto but known to all parties, and the Exhibits form an integral part of this Agreement. 1.2 Institution and Principal Investigator agree to use their best efforts and professional expertise to perform the Clinical Trial in accordance with the Protocol, all applicable legal and regulatory requirements, the identified timelines and the terms and conditions of this Agreement. Institution and Principal Investigator may not start the clinical trial without prior approval of the ethics committee, notifications and further legally required approvals. 1.3 In the event that the Principal Investigator becomes no longer affiliated with Institution, Institution shall provide written notice to Sponsor and CRO as soon as possible and at the latest within three (3) calendar days of such departure. Sponsor or CRO on behalf of the Sponsor shall have the right to approve any new Principal Investigator designated by Institution. The new Principal Investigator shall be required to agree to the terms and conditions of this Agreement. In the event Sponsor does not approve such new Principal Investigator, Sponsor may terminate this Agreement in accordance with Section 2.2 below and Institution shall take all necessary steps to accommodate Sponsor’s decision. If Principal Investigator is to be temporarily absent from Institution for more than 10 days, but not more than 14 days, Institution will designate a Sub-investigator to temporarily supervise the Study on the Principal Investigator’s behalf. Institution will document this designation and notify Sponsor in writing of such designation prior to its commencement. If Principal Investigator is, or is to be, absent for more than 14 days, Sponsor may terminate Agreement if Institution and Sponsor cannot agree on a replacement Principal Investigator within a 14-day period. 1.4 Institution and Principal Investigator may appoint such other individuals and investigational staff as they may deem appropriate as co-investigator or investigational staff to assist in the conduct of the Clinical Trial. All co-investigators and investigational staff will be adequately qualified, timely appointed and an updated list will be maintained. Principal Investigator shall be responsible for leading such team of co-investigators and investigational staff, who in all respect shall be bound to the same terms and conditions as the Principal Inves...
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Performance of the Clinical. Trial 1.1 The parties agree that the Protocol, including any subsequent Protocol amendments, if not attached hereto but known to all parties, and the Exhibits form an integral part of this Agreement. 1.2 Institution and Principal Investigator agree to use their best efforts and professional expertise to perform the Clinical Trial in accordance with the Protocol, all applicable legal and regulatory requirements, the identified timelines and the terms and conditions of this Agreement. Institution
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Performance of the Clinical. Trial 1.1 Institution and Principal Investigator agrees to use best efforts and professional expertise to perform the Clinical Trial in accordance with the Protocol, all applicable legal and regulatory requirements, such as regulation No 140/1998 subsequently amended, regulation No. 428/2002 subsequently amended, regulation No.576/2004 subsequently amended, approved by State Institute for Drug Control No. 2010/1914/SBLKS on 24.3.2011, approved by Ethic Commitee No. EK/10/37 on 9.12.2010 and with the identified timelines and the terms and conditions of this Agreement. 1.2 Institution may appoint such other individuals and investigational staff as it may deem appropriate as co-investigator and investigational staff to assist in the conduct of the Clinical Trial. All co-investigators and investigational staff will be adequately qualified, timely appointed and an updated list will be maintained. Names of co-investigators: MUDr.Milena Surová, MUDr.Monika
Sample 1
Performance of the Clinical. Trial 1.1 The parties agree that the Protocol, including any subsequent Protocol amendments, if not attached hereto but known to all parties, and the Exhibits form an integral part of this Agreement. 1.2 Institution and Principal Investigator agree to use their best efforts and professional expertise to perform the Clinical Trial in accordance with the Protocol, all applicable legal and regulatory requirements, the identified timelines and the terms and conditions of this Agreement. Institution and Principal Investigator may not start the clinical trial without prior approval of the ethics committee, notifications and further legally required approvals. 1.3 In the event that the Principal Investigator becomes no longer affiliated with Institution, Institution shall provide written notice to Sponsor and CRO as soon as Zdravotnické zařízení bere na vědomí, že ZADAVATEL spolu s touto smlouvou podepíše současně také smlouvu s hlavním zkoušejícím ohledně činností, které má hlavní zkoušející během klinického hodnocení vykonávat a které jdou nad rámec činností, za které je na základě této smlouvy, odpovědné zdravotnické zařízení. V této smlouvě s hlavním zkoušejícím bude specifikována odměna pro hlavního zkoušejícího a členy týmu, provádějícího klinické hodnocení, za provádění těchto činností. Zdravotnické zařízení bere na vědomí a souhlasí s xxx, že odměna za služby poskytované pro účely klinického hodnocení hlavním zkoušejícím a členy týmu provádějícího klinické hodnocení na základě těchto samostatných smluv, může být vyplacena přímo hlavnímu zkoušejícímu a členům týmu provádějícího klinické hodnocení. Se nyní proto, s ohledem na výše uvedené skutečnosti a vzájemné sliby a ujednání vyjádřené v této Smlouvě, Strany dohodly následovně: 1. Provedení Klinického hodnocení 1.1 Strany souhlasí, že Protokol, včetně veškerých následných dodatků k Protokolu, pokud nejsou k této Smlouvě přiloženy, ale jsou všem stranám známy, jakož i přílohy této Smlouvy tvoří její nedílnou součást. 1.2 Zdravotnické zařízení a Hlavní zkoušející souhlasí, že vyvinou maximální úsilí a využijí odbornou způsobilost při provádění Klinického hodnocení v souladu s Protokolem, všemi platnými právními a regulačními požadavky, určenými časovými harmonogramy a podmínkami této Smlouvy. Zdravotnické zařízení a Hlavní zkoušející nesmí zahájit Klinické hodnocení bez předchozího souhlasu etické komise, oznámení a dalších souhlasů nutných dle právních předpisů. 1.3 V případě, že Hlavní zkoušející již nebu...
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Related to Performance of the Clinical

  • PERFORMANCE OF THE CONTRACT II.1.1 The Contractor shall perform the Contract to the highest professional standards. The Contractor shall have sole responsibility for complying with any legal obligations incumbent on him, notably those resulting from employment, tax and social legislation.

  • PERFORMANCE OUTCOMES 8 A. CONTRACTOR shall achieve performance objectives, tracking and reporting Performance 9 Outcome Objective statistics in monthly programmatic reports, as appropriate. ADMINISTRATOR 10 recognizes that alterations may be necessary to the following services to meet the objectives, and,

  • Performance of Products and Services The Contractor acknowledges that only Project Persons shall perform the Products and Services under this Agreement.

  • Performance of the Work The Contractor shall perform all of the Work required for the complete and prompt execution of everything described or shown in, or reasonably implied from the Contract Documents for the above referenced Project.

  • Standard of Care; Performance of Employees Consultant shall perform all Services under this Agreement in a skillful and competent manner, consistent with the standards generally recognized as being employed by professionals in the same discipline in the State of California. Consultant represents and maintains that it is skilled in the professional calling necessary to perform the Services. Consultant agrees that all employees and subconsultants shall have sufficient skill and experience to perform the Services assigned to them. Finally, Consultant represents that it, its employees and subconsultants shall have all licenses, permits, qualifications and approvals of whatever nature that are legally required to perform the Services, including a City Business License, and that such licenses and approvals shall be maintained throughout the Term of this Agreement. As provided for in the indemnification provisions of this Agreement, Consultant shall perform, at its own cost and expense and without reimbursement from the City, any services necessary to correct errors or omissions which are caused by the Consultant’s failure to comply with the standard of care provided for herein. Any employee of the Consultant or its sub-consultants who is determined by the City to be uncooperative, incompetent, a threat to the adequate or timely completion of the Project, a threat to the safety of persons or property, or any employee who fails or refuses to perform the Services in a manner acceptable to the City, shall be promptly removed from the Project by the Consultant and shall not be re-employed to perform any of the Services or to work on the Project.

  • Performance of the Services In addition to the Common Articles, it is specified that:

  • 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.

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

  • Performance of Services The Contractor is responsible for fully meeting all obligations set forth in the Contract and for providing Product in accordance with the Contract or any Authorized User Agreement.

  • Performance Orders A Performance Order:

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