Site Monitoring. Return visits to the site may be undertaken to allow the completion of work listed above, or for the express purpose of monitoring the site. Changes to the disposition or physical nature of seabed remains should be noted, based on photographic, video or measured survey. This work will directly inform on the processes acting upon the site and help the management of the site in the future. Additional work may also be undertaken in the form of desk-based research as a means to increase basic knowledge of the site and to provide further context to the work described above. Full details of all HPA tiers and associated tasks are included in Annex 2. Name: Signature: Name: Signature: Name: Signature: Name: Signature:
Site Monitoring. The Project will be monitored by the control room on a 24/7 basis.
Site Monitoring. As a member of Feeding America, FTV is required to conduct a site-monitoring visit of each program at least once every two years.
Site Monitoring. Develop and Implement monitoring plan E Conduct monitoring (Source document verification, drug accountability, regulatory document review, eCRF review, supply inventory, etc.) E Identify and report non-compliance E Provide written monitoring reports E Conduct Site close-out procedure (final source document verification, drug accountability, regulatory document review, eCRF review, study supply disposition, etc.) E
Site Monitoring. During the term of the New License and any subsequent annual licenses, Chelan PUD, in consultation with the RRCF, shall monitor the Historic Properties identified in the APE and update site information using a rotation system that prioritizes sites based on current assessments of ongoing Project effects. Chelan PUD shall revisit sites every one, three, five or fifteen years, as described in Section 5.2 of Chapter 8 of the Comprehensive Plan.
Site Monitoring. The appointed contractors will undertake the necessary monitoring to comply with the requirements of these DGN and the contract plus any additional consent requirements that emerge from engagement and approval from statutory bodies. Monitoring may include: monitoring the effectiveness of mitigation ; monitoring the impact of the Ground Investigation works; and taking other actions as may be necessary to enable compliance. Monitoring, together with provisions for any corrective action required, will be implemented under the contract.
Site Monitoring. Art Auction Analytics reserves the right to view, monitor, and record activity on the site without notice or further permission from you, to the fullest extent permitted by applicable law. We reserve the right to discontinue access to the site either with or without notice if we have a reasonable basis to believe that a user is accessing or using services in violation of these terms of use, in addition to any other rights and remedies that may be available.
Site Monitoring. Before study initiation, Karyopharm personnel (or designated contract research organization [CRO]) will review the protocol with the Investigators and their staff (e.g., at a site initiation visit). During the study, the monitor will visit the site regularly to check the completeness of patient records, accuracy of entries on the CRFs, adherence to the protocol and to Good Clinical Practice (GCP), progress of enrollment, and to ensure that study treatment is being stored, dispensed, and accounted for according to specifications. Key study personnel must be available to assist the monitor during these visits. The Investigator must maintain source documents for each patient in the study, consisting of case and visit notes (hospital or clinic medical records) containing demographic and medical information, laboratory data, ECGs, and the results of any other tests or assessments. All information recorded on CRFs must be traceable to source documents in the patient's file. The Investigator must also keep the original signed ICF (a signed copy is given to the patient). The Investigator must give the monitor access to all relevant source documents to confirm their consistency with the CRF entries. Karyopharm monitoring standards require full verification for the presence of informed consent, adherence to the inclusion/exclusion criteria and documentation of SAEs. Additional checks of the consistency of the source data with the CRFs are performed according to the study-specific monitoring plan.
Site Monitoring. We have the right at any and all times to monitor your web site or channel in order to determine if you are in compliance with the terms of this Agreement. We shall have no obligations with respect to the content available on your web site or channel, including, but not limited to, any duty to review or monitor any such content. We reserve the right to discontinue the Basic Benefits or any Additional Features if we determine (in our sole discretion) that your web site or channel violates any of the above-stated terms or is objectionable, offensive or otherwise violates a law or our policy.
Site Monitoring. Members and site supervisors must complete a site monitoring survey in the winter or spring, to be sent by CLEC staff. CLEC staff will also conduct annual site monitoring visits for selected sites. Site monitoring visits may be in-person or virtual with both members and site supervisors. The member is required to log their service hours using the America Learns timekeeping system. The member may only count hours while serving at their host or service site, on their campus, while tele- serving during COVID-19, or during a service project or training. Members may not count travel time to and from a service site as service hours unless they are discussing their project with staff or other program participants while in travel status. The member is responsible for ensuring they are able to complete their full term of service before their end date. The member must work with their supervisor to ensure that enough time is served during each pay period to complete the allotted hours. Members will need to plan around any days their site is closed (e.g., holidays) or during planned approved vacation as they will not be accruing hours during that time. • Members must submit their timesheet on the 1st and 16th of each month (e.g., September 1-15 - due September 16th; September 16-30 - due October 1st). • Timesheets must be approved by the site supervisor within 4 days (by the 5th and 20th of each month) after members submit their timesheet. • Supervisors are responsible for knowing their member’s day-to-day activities as reflected on their timesheets. By approving the member’s timesheet, the supervisor certifies the accuracy of the total hours served against their records. Failure to ensure accuracy and/or timely submissions of member timesheets may result in reduced allocations to the host site in the future. • Three or more missing timesheets may be cause for termination. The Member is encouraged to take 30 to 60 minutes for lunch each day. Lunch breaks may not be counted as direct service or be included on timesheets under any service category. • Full-time members are expected to serve eight hours per day during general business hours. Some weekend hours are expected for events, conferences, and National Days of Service. Student Fellows, part-time, and half-time members will have varying hours. • Members may not log service hours in advance. • Health and wellness are a top priority for CLEC. Therefore, members should not be scheduled for more than the following hour...
