Performance of Activities. The Nurse Representative shall notify her/his immediate supervisor prior to performing permitted Nurse Representative duties on work time. If, in the supervisor’s discretion, the permitted activity would interfere with the work of the Nurse Representative or other employees, the Nurse Representative will arrange with the responsible supervisor(s) for a mutually satisfactory time to perform the requested activity.
Performance of Activities. Data Recipient may use and disclose the Limited Data Set only (1) in the performance of the research activities (the “Activities”) as detailed in Attachment B to this Agreement, or (2) subject to the provisions of Section 3.d, as otherwise required by law.
Performance of Activities. In the event of a termination under this Article 2, (a) Investigator will immediately stop enrolling subjects into the Study and cease conducting Study procedures and treatment with the Study Drug on subjects already entered into the Study, to the extent medically advisable, and (b) Institution and/or Investigator will (i) furnish to Sponsor all Study Data and all CRFs, completed or partially complete, as of the effective date of termination, and (ii) return to Sponsor all Study Drug that were furnished to Institution or Investigator, in accordance with Sponsor’s instruction, except for records or samples which the Institution and/or Investigator is required by law to retain. Within thirty (30) days of termination of this Agreement or completion of the Study (whichever (b) Vykonávání činností. V případě ukončení Smlouvy podle tohoto Článku 2
(a) Zkoušející ihned ukončí nábor subjektů do Studie, přestane vykonávat úkony pro Studii a podávat Hodnocený přípravek subjektům již zařazeným do Studie , bude-li to z lékařského hlediska vhodné, a (b) Zdravotnické zařízení a/nebo Zkoušející (i) dodají Zadavateli veškerá Studijní data a veškeré formuláře CRF kompletně nebo i jen částečně vyplněné k datu účinnosti ukončení Smlouvy a (ii) podle pokynů Zadavatele vrátí Zadavateli veškeré dávky Hodnoceného přípravku, které byly Zdravotnickému zařízení nebo Zkoušejícímu dodány, s výjimkou záznamů nebo vzorků, které si jsou Zkoušející a/nebo Zdravotnické zařízení ze zákona povinni ponechat. Do třiceti (30) dnů od ukončení Smlouvy nebo comes first), Investigator will submit final written reports to Sponsor as specified in the Protocol. After termination of this Agreement or suspension of the Study at the Institutionfor any reason, all Parties shall continue activities under this Agreement solely as deemed necessary by mutual agreement of the Parties based on reasonable medical judgment to protect the health of subjects participating in the Study. This Section 2.5 survives termination of this Agreement. dokončení Studie (podle toho, co nastane dříve) Zkoušející předloží Zadavateli závěrečné písemné zprávy stanovené v Protokolu. Po ukončení této Smlouvy nebo po pozastavení Studie ve Zdravotnickém zařízení bez ohledu na důvod budou všechny Strany pokračovat ve své činnosti podle této Smlouvy výhradně v rozsahu, v jakém to bude nezbytné a na jakém se Strany dohodnou s přihlédnutím k přiměřenému lékařskému úsudku v zájmu ochrany zdraví subjektů účastnících se Studie. Tento bod 2....
Performance of Activities. (a) Performance of the Activities shall be coordinated with a representative of Owner to minimize unreasonable interference with normal operation of the Premises. All Activities at the Premises shall be performed during normal business hours or at such other times and on such days of the week as Owner shall determine in its reasonable discretion and shall be performed in a manner that will not have any material adverse effect on Owner, or any other person or entity granted rights of use and occupancy through Owner, their respective agents, employees or invitees, or all of them.
(b) Upon completion of the Activities, Entrant shall, at its sole cost and expense, promptly remove and dispose of off of the Premises, in accordance with all Environmental Laws, all equipment, material, soil, water and debris which exists on the Premises as a result of Entrant’s collection of samples from the Premises.
(c) Entrant shall use commercially reasonable efforts to cause its environmental consultant, to reasonably cooperate and coordinate with Owner for the collection of samples of any testing of soils or ground water at the Premises in accordance with Section 6 of this Agreement.
(d) All Activities performed at the Premises by Entrant or the Permitted Parties shall, once begun, be completed with reasonable diligence and paid for in full by Entrant, free and clear of all mechanic’s or other liens and encumbrances, and shall be performed in accordance with all applicable statutes, ordinances, rules, regulations, orders and requirements of any Governmental Authority, including without limitation, Environmental Laws. All Activities performed by Entrant or the Permitted Parties shall be done in a good and workmanlike manner, and, subject to Section 6 of this Agreement, in such a manner so as not to cause any unreasonable damage to the Premises or unreasonable interference with the use and occupancy of the Premises by Owner, or any other person or entity granted rights of use and occupancy through Owner, or their respective agents, employees or invitees. Entrant shall restore, repair or replace, as the case may be, any damage to the Premises caused by the Activities to substantially the same condition as existed at the time the Activity which caused such damage commenced.
Performance of Activities. Data User may use and disclose the Limited Data Set received from Covered Entity only in connection with the performance of Data User shall limit the use or receipt of the Limited Data Set to the following individuals or classes of individuals who need the Limited Data Set for the performance of the Activities: For HIV-related information, Data User hereby acknowledges and agrees that Covered Entity has notified Data User that it is required to comply with the confidentiality, disclosure and re-disclosure requirements of 10 NYCRR Part 63.
Performance of Activities. Data User may use and disclose the Limited Data Set received from Covered Entity only in connection with the performance of the activities described on the “Request to Access Health Information by Use of a Limited Data Set” attached to this Agreement (the “Activities”). Data User shall limit the use or receipt of the Limited Data Set to the individuals or classes of individuals described on the attached “Request to Access Health Information by Use of a Limited Data Set” who need the Limited Data Set for the performance of the Activities.
Performance of Activities. Data User may use and disclose the Limited Data Set received from Covered Entity only in connection with the performance of the: Research Activities Public Health Activities Health Care Operations Provided in Exhibit A, attached to this Agreement Provided under Agreement (the “Activities”)ii
Performance of Activities. Data User may use and disclose the Data Set received from Covered Entity only in connection with the performance of the following research activities: Completion of the Specific Aims of the XXX initiative and any adjunct research activities generated by the XXX initiative.
Performance of Activities. Data User may use and disclose the Limited Data Set received from Covered Entity only in connection with the performance of Burn Model System research activities. Data User shall limit the use or receipt of the Limited Data Set to members of the Burn Model Systems research team at [name of Burn Model System] and certain individuals within these institutions who are responsible for overseeing research activities.
Performance of Activities. Data User may use and share findings resulting from analysis of the Limited Data Set received from Covered Entity only in connection with the performance of the evaluation/research activities (“Activities”) described below NCOA requires a high-level overview of the goals, objectives, research designs/approach, measures, and any plans to merge or link NCOA data sources to other data sources (e.g. national health data sources) written in laymen’s terms in the section below. Attach additional information, if needed. An Institutional Review Board (IRB) approval document from the Data User’s institution or other trusted entity is required, if applicable to the Data User’s institution. Please attach a copy.
