Study Personnel. Site and Training of 3. Studijní pracoviště a proškolení personálu.
Study Personnel. Site represents that, during the course of the Study, all subinvestigators, employees, contractors, affiliates, agents and any other persons performing services for the Study (together as “Personnel”) shall have the appropriate training, information, licenses, approvals, and certifications necessary to safely, adequately and lawfully perform the Study in accordance with this Agreement. Further, Site shall be responsible to ensure that the Personnel 1.3 Pracovníci provádějící studii: Místo výkonu klinického hodnocení prohlašuje, že po celou dobu provádění Studie všichni spoluzkoušející, zaměstnanci, dodavatelé, pobočky, zástupci a jakékoli jiné osoby, které budou poskytovat služby pro účely studie (společně jen jako „Pracovníci“), budou mít řádnou kvalifikaci, informace, oprávnění, souhlasy a certifikace potřebné k bezpečnému, řádnému a zákonnému provádění studie v souladu s touto Smlouvou. have read and understood the Protocol and shall perform their activities and fulfill their obligations in a timely and competent manner. Dále musí Místo výkonu klinického hodnocení zajistit, aby si pracovníci přečetli protokol, chápali jeho obsah a vykonávali svou činnost a plnili své povinnosti včas a správným způsobem.
Study Personnel. Upon the prior written consent of SPONSOR, INSTITUTION may use other employees of INSTITUTION and contractors, including the personnel of any Study facility named in PRINCIPAL INVESTIGATOR’s FDA Form 1575, to perform any Study-related services under this Agreement (together with PRINCIPAL INVESTIGATOR, “Study Personnel”). INSTITUTION shall ensure that: Adequate numbers of qualified Study Personnel are assigned to the Studies to meet its obligations under this Agreement; All Study Personnel perform their Study responsibilities and fulfill their obligations under this Agreement; All Study Personnel have the necessary licenses and certifications as may be required to perform their Study responsibilities, and shall, upon request of SPONSOR, provide such documented evidence of any such licenses and certifications; All Study Personnel receive the necessary information, education, and training in any applicable regulatory requirements, proper performance of the Protocols, GCP Guidelines, and any other applicable guidelines relevant to the Studies and performance of the Protocols, and shall, upon request of SPONSOR, provide such documented evidence of any such education and training; and
Study Personnel. (a) USOR shall cause each Investigator to complete, sign and deliver to BIND or its designee FDA Form 1572 prior to commencement of the Study at any such Investigator’s Site. In the event an Investigator becomes unwilling or unable to perform the duties required by this Agreement and the Protocol, USOR shall reasonably cooperate with BIND to find a replacement; provided, however, that such Investigator shall continue to be bound by the surviving provisions of this Agreement set forth in Section 16.6 applicable to him/her. If an acceptable replacement is not found within thirty (30) days, BIND may terminate the Study at such Investigator’s Site.
Study Personnel. Institution will arrange for qualified medical, technical, laboratory, clerical and other personnel, including Sub-investigators and permitted subcontractors pursuant to Section 10.6, if applicable, that are necessary, desirable, and available to support and carry out Institution’s obligations under this Agreement (collectively, the “Study Personnel”). Institution will be solely responsible for paying Study Personnel. Further, Institution will ensure that before commencing any work on the Study, all Study Personnel are subject to written obligations to Institution under which they (a) are bound to obligations of confidentiality and non-use with respect to Confidential Information (as defined in Section 5) that are consistent with the terms of this Agreement; and (b) assign and otherwise effectively vest in Institution any and all rights that such Study Personnel might otherwise have in the results of their work without any obligation of Sponsor to pay any royalties or other consideration to such Study Personnel. 2.3
Study Personnel. THM shall ensure that all Study Personnel shall: (i) have the appropriate experience and qualifications to participate in and perform the Study pursuant to the Research Program; and (ii) comply with the terms and conditions set forth in this Agreement.
Study Personnel. 6.1.1 [***] The [***] will be [***] for the [***] of this [***].
Study Personnel. Upon the prior written consent of SPONSOR, INSTITUTION may use other employees of INSTITUTION and contractors, including the personnel of any Study facility named in PRINCIPAL INVESTIGATOR’s FDA Form 1575, to perform any Study-related services under this Agreement (together with PRINCIPAL INVESTIGATOR, “Study Personnel”). INSTITUTION shall ensure that:
Study Personnel
