Issue Diagnosis Sample Clauses

Issue Diagnosis. Moogsoft will work with the End User Technical Contacts to understand and document an Issue and reproduce it where appropriate. Furthermore: a) End user will provide all log, configuration, and related files and settings required for analysis; b) End User will allow Moogsoft to view and record the operation of the Product if needed to understand or communicate the nature of the Issue and steps to diagnose and/or remediate it; c) Moogsoft may request tests be performed, such tests will be performed by the End User Technical Contact; d) In some cases, it may be necessary to wait for non-reproducible, intermittent, problems to re-occur with additional logging enabled. End User Technical Contact will monitor the Product and report to Moogsoft when it has re-occurred and provide results; and e) When End User systems are hosted on Moogsoft’s SaaS infrastructure, Moogsoft Support Services will access the systems directly, including logging in via the Product User Interface.
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Issue Diagnosis. Vitria will work with the End User Technical Contacts to understand and document an Issue and reproduce it where appropriate. Furthermore: a) End user will provide all log, configuration, and related files and settings required for analysis; b) End User will allow ▇▇▇▇▇▇ to view and record the operation of the Product if needed to understand or communicate the nature of the Issue and steps to diagnose and/or remediate it; c) Vitria may request tests be performed, such tests will be performed by the End User Technical Contact; d) In some cases, it may be necessary to wait for non-reproducible, intermittent, problems to re-occur with additional logging enabled. End User Technical Contact will monitor the Product and report to Vitria when it has re-occurred and provide results; and e) When End User systems are hosted on Moogsoft’s SaaS infrastructure, VitriaSupport Services will access the systems directly, including logging in via the Product User Interface.
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Issue Diagnosis. Customer and CSG will be actively engaged following Customer’s trouble report and will use commercially reasonable efforts to identify the problem and diagnose the issue in order to expedite dispatch of the proper Hardware Components.
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Related to Issue Diagnosis

  • Medical Verification The Town may require medical verification of an employee’s absence if the Town perceives the employee is abusing sick leave or has used an excessive amount of sick leave. The Town may require medical verification of an employee’s absence to verify that the employee is able to return to work with or without restrictions.

  • How to File an Appeal of a Prescription Drug Denial For denials of a prescription drug claim based on our determination that the service was not medically necessary or appropriate, or that the service was experimental or investigational, you may request an appeal without first submitting a request for reconsideration. You or your physician may file a written or verbal prescription drug appeal with our pharmacy benefits manager (PBM). The prescription drug appeal must be submitted to us within one hundred and eighty (180) calendar days of the initial determination letter. You will receive written notification of our determination within thirty (30) calendar days from the receipt of your appeal. Your appeal may require immediate action if a delay in treatment could seriously jeopardize your health or your ability to regain maximum function, or would cause you severe pain. To request an expedited appeal of a denial related to services that have not yet been rendered (a preauthorization review) or for on-going services (a concurrent review), you or your healthcare provider should call: • our Grievance and Appeals Unit; or • our pharmacy benefits manager for a prescription drug appeal. Please see Section 9 for contact information. You will be notified of our decision no later than seventy-two (72) hours after our receipt of the request. You may not request an expedited review of covered healthcare services already received.

  • Human Leukocyte Antigen Testing This plan covers human leukocyte antigen testing for A, B, and DR antigens once per member per lifetime to establish a member’s bone marrow transplantation donor suitability in accordance with R.I. General Law §27-20-36. The testing must be performed in a facility that is: • accredited by the American Association of Blood Banks or its successors; and • licensed under the Clinical Laboratory Improvement Act as it may be amended from time to time. At the time of testing, the person being tested must complete and sign an informed consent form that also authorizes the results of the test to be used for participation in the National Marrow Donor program.

  • Random Drug Testing All employees covered by this Agreement shall be subject to random drug testing in accordance with Appendix D.

  • Clinical 1.1 Provides comprehensive evidence based nursing care and individual case management to a specific group of patients/clients including assessment, intervention and evaluation. 1.2 Undertakes clinical shifts at the direction of senior staff and the Nursing Director including participation on the on-call/after-hours/weekend roster if required. 1.3 Responsible and accountable for patient safety and quality of care through planning, coordinating, performing, facilitating, and evaluating the delivery of patient care relating to a particular group of patients, clients or staff in the practice setting. 1.4 Monitors, reviews and reports upon the standard of nursing practice to ensure that colleagues are working within the scope of nursing practice, following appropriate clinical pathways, policies, procedures and adopting a risk management approach in patient care delivery. 1.5 Participates in ▇▇▇▇ rounds/case conferences as appropriate. 1.6 Educates patients/carers in post discharge management and organises discharge summaries/referrals to other services, as appropriate. 1.7 Supports and liaises with patients, carers, colleagues, medical, nursing, allied health, support staff, external agencies and the private sector to provide coordinated multidisciplinary care. 1.8 Completes clinical documentation and undertakes other administrative/management tasks as required. 1.9 Participates in departmental and other meetings as required to meet organisational and service objectives. 1.10 Develops and seeks to implement change utilising expert clinical knowledge through research and evidence based best practice. 1.11 Monitors and maintains availability of consumable stock. 1.12 Complies with and demonstrates a positive commitment to Regulations, Acts and Policies relevant to nursing including the Code of Ethics for Nurses in Australia, the Code of Conduct for Nurses in Australia, the National Competency Standards for the Registered Nurse and the Poisons Act 2014 and Medicines and Poisons Regulations 2016. 1.13 Promotes and participates in team building and decision making. 1.14 Responsible for the clinical supervision of nurses at Level 1 and/or Enrolled Nurses/ Assistants in Nursing under their supervision.