The Principal Investigator. 5.1. Xxxxx X. Xxxxx MD, PhD of the Medical Center (hereinafter: “the Principal Investigator”) has agreed to serve as the principal investigator of the Trial
The Principal Investigator for the Contract or Grant shall be responsible for executing the project in conformance with the approved budget.
The Principal Investigator and the Institution must use the wording below when acknowledging a grant from XXXXX. When appropriate, such as in a scientific journal article, the grant number must be included. ‘Funding for xxx - grant number was obtained from XXXXX UK.’
The Principal Investigator. Xxxxxx Xxx Xxxx – will coordinate the entire project and will have full responsibility of the project development.
The Principal Investigator. Mr/Ms/Mrs................ ANNEX II RESEARCH TEAM: PI: PARTNERSHIP: ANNEX III The sponsor and the investigator confirmed by this clause that the device evaluated in this study will be used in an indication for which it is authorized in Spain, in the patient population for which it is authorized in Spain, in terms of use authorized in Spain and that their use corresponds to the clinical care standard at the CENTRE/HOSPITAL.
The Principal Investigator i. CV Higher education • MA in Germanic Philology, Department of Germanic Studies, Faculty of Arts, University of Bologna (Italy). Masters thesis ‘The diffusion of the Visio Tnugdali in Germanic literatures of the Middle Ages’ (cum laude, 19 November 1993). • PhD in Middle Dutch Literature, Department of Dutch Literature, Faculty of Arts, University of Leiden (the Netherlands). Supervisor: Prof. xx Xxxxx xxx Oostrom. Thesis defended on 17 May 2000. Title: Italiaanse deugden en ondeugden. Dirc Potters Xxxxx der doechden en de Italiaanse Xxxxx di Virtù (Italian Virtues and Vices. Xxxx Xxxxxx’x Xxxxx der doechden and the Italian Xxxxx di Virtù). This doctoral thesis offers a comparative study of the Middle Dutch text Xxxxx der doechden, by the Middle Dutch writer Xxxx Xxxxxx (1370–1428), and the Italian didactic treatise Xxxxx di virtù, written in Bologna in the first decades of the 14th century. The study attempts to define the relationship between the Middle Dutch and the Italian. The textual and philological analysis is completed by a detailed study of the life of Xxxx Xxxxxx, who resided in Rome between 1411 and 1412, the first Middle Dutch writer to undertake such a journey. Work experience and research positions • Research Institute for Medieval Studies, University of Leiden (the Netherlands). Coordinator of research and teaching activities, 1 April 1999 to 1 September 1999.
The Principal Investigator. For sake of clarity, the Principal Investigator is an employee of Institution and will be named in Exhibit A. The Principal Investigator represents and certifies that he or she has read and understands the Investigator’s protocol and brochure. The Principal Investigator is not a party but must read, sign and acknowledge the entire agreement. During the Study, the Institution shall immediately notify SPONSOR in writing at such time as it becomes aware that the Principal Investigator plans to leave the Institution or shall be unable to complete the Study. If the Institution and SPONSOR are unable to agree on an acceptable substitute investigator within fifteen (15) business days following such notice, SPONSOR may terminate this Agreement pursuant to Section 24.
The Principal Investigator the SPONSOR and the monitors and auditors will observe the internal procedural rules of the HOSPITAL and the FOUNDATION, which will be provided by the latter, and also the indications on the performance of the CLINICAL TRIAL given by the CEIm responsible for monitoring them.
The Principal Investigator shall be supported in the execution of the Clinical investigation by the healthcare and non-healthcare personnel and by any contractors engaged by the Entity, as appointed by the Entity and operating under its responsibility for all aspects pertaining to this Clinical investigation, who are qualified to conduct the Clinical investigation, and who have previously received adequate training as provided for in the applicable laws, by the Sponsor/CRO and who have declared their willingness to take part in the Clinical investigation (the Co-investigators). Without affecting the foregoing, the definition of “Investigators” does not include any medical or non-medical personnel who perform proprietary institutional activities in the context of the Clinical investigation (for example pharmacists, IT technicians).
The Principal Investigator shall keep all of the Case Report Forms (CRF), duly compiled, in accordance with the terms and conditions of the Protocol for the Clinical investigation and with the applicable regulations, in printed or digital form, and in any case they shall be delivered promptly in accordance with the GCP, by the date indicated in the Clinical investigation Protocol.
