Monthly Discussion Requirements Sample Clauses

Monthly Discussion Requirements. All discussions with participants must be documented in concise detail in the participant’s case notes, within the Department’s case management system (WISITS). Communications by email or text meet the monthly discussion requirements, but are still subject to case note and discussion topic requirements. Topics of conversation for monthly contact shall include, but are not limited to: A review and documentation of progress on implementation of the ISSP. Documentation of any usage and effectiveness of the 24-hour emergency backup plan. A review budget spending patterns, including an analysis of any over- and under-utilization of services. Assessment of the quality of services, access to supports, and functionality of goods in accordance with the quality assurance section of the ISSP and any applicable IRIS service standards. A review of any incidents or events impacting the participant’s health, welfare, or ability to fully access and utilize support as identified in the ISSP. A review any conflict of interest issues and any health or safety issues. The progress towards achieving outcomes, including employment if applicable. Other concerns or challenges as noted by the participant or legal decision maker.
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Monthly Discussion Requirements. All discussions with participants must be documented in concise detail in the participant’s case notes, within the Department’s case management system (WISITS). The monthly contact with the participant must be either telephonically or by live video. Communications by email or text do not meet the monthly contact requirements. Topics of conversation for monthly contact shall include, but are not limited to: A review and documentation of progress on implementation of the ISSP. Documentation of any usage and effectiveness of the 24-hour emergency backup plan. A review budget spending patterns, including an analysis of any over- and under-utilization of services. Assessment of the quality of services, access to supports, and functionality of goods in accordance with the quality assurance section of the ISSP and any applicable IRIS service standards. A review of any incidents or events impacting the participant’s health, welfare, or ability to fully access and utilize support as identified in the ISSP. A review any conflict of interest issues and any health or safety issues. The progress towards achieving outcomes, including employment if applicable. Other concerns or challenges as noted by the participant or legal decision maker. …

Related to Monthly Discussion Requirements

  • Submission Requirements The Contractor shall submit inventory disposal schedules to the Plant Clearance Officer no later than—

  • Admission Requirements USERs and Participants are subject to the administrative and technical supervision and control of CONTRACTOR; and will comply with all applicable rules of CONTRACTOR and DOE with regard to admission to and use of the User Facility, including safety, operating and health- physics procedures, environment protection, access to information, hours of work, and conduct. Participants shall execute any and all documents required by CONTRACTOR acknowledging and agreeing to comply with such applicable rules of CONTRACTOR. Participants will not be considered employees of CONTRACTOR for any purpose.

  • Data Submission Requirements As part of its registration and sponsorship of Registered Names in the Registry TLD, Registrar shall submit to the Registry System complete data as required by technical specifications of the Registry System that are made available to Registrar from time to time. Registrar hereby grants Registry Operator a non-exclusive, royalty free, non-transferable, limited license to such data for propagation of and the provision of authorized access to the TLD zone files and as otherwise required for Registry Operator to meet its obligations to ICANN and/or for Registry Operator’s operation of the Registry TLD.

  • Notification Requirements 1. If the Family Leave is foreseeable, the employee must provide the agency/department with thirty (30) calendar days notice of his or her intent to take Family Leave.

  • GRADUATION REQUIREMENTS I understand that in order to graduate from the program and to receive a certificate of completion, diploma or degree I must successfully complete the required number of scheduled clock hours as specified in the catalog and on the Enrollment Agreement, pass all written and practical examinations with a minimum score of 80%, and complete all required clinical hours and satisfy all financial obligations to the College. Initial

  • Publication Requirements Those seeking to include renderings of more than 10 images from the UND Biometrics Database in reports, papers, and other documents to be published or released must first obtain approval in writing from the UND Principal Investigator. In no case should the face images be used in a way that could cause the original subject embarrassment or mental anguish.

  • Admission and Graduation Requirements A. The receiving institution’s admission and program admission requirements apply to both direct entry students and to students who transfer under this agreement.

  • Application Requirements This application shall contain, as a minimum, a sketch showing the location of proposed facilities; a description, sketch, manufacturer’s brochure, etc. of the proposed facilities; and a description of the operation proposed. (11-28-90) 101. -- 199. (RESERVED)‌ 200. OPERATIONAL AGREEMENT.‌‌

  • Notice and Variation Requirements (a) An employee shall give no less than eight weeks written notice to the employer of:

  • Certification Requirements The applicant will provide Vista Laboratories, Inc. with all product information for the evaluation of the product to be certified and warrant that the information provided is accurate and complete so that Vista Labs may perform the services requested. If the product was tested at an external laboratory, the applicant must provide the complete test report to Vista Labs. If the external testing facility is not ISO 17025 accredited, or does not have the proper scope, Vista Labs must determine if the test report can be used for certification activities. The applicant’s information is used to perform a product review and evaluation to determine the product’s compliance to the specific certification requested. Throughout the process, the client agrees to make claims regarding certification consistent with the scope of certification. The applicant agrees to supply the required number of product samples, to be determined by Vista Labs, to the laboratory for testing, measurement, and evaluation purposes. The client understands that certain tests may damage or destroy the sample and acknowledge that Vista Labs is not responsible for such damages. Samples will be returned only upon request by the applicant and at the applicant’s expense, after the completion of certification. Samples will be disposed of after six months if not requested for return by applicant. The product is ineligible for certification if it has been modified by the client after testing or certification. Changes to the product must be approved by Vista Laboratories. Vista Labs reserves the right to re- evaluate the product as a result of information that raises questions concerning the conformance of the product. Certified products maintain fulfilment of product requirements if the certification applies to ongoing production. If the client provides copies of the certification documents to other parties, the documents are reproduced in their entirety, or as specified in the certification scheme. In making reference to its product certification in media, such as brochures or advertisement, the client complies with the requirements of the Vista Labs or as specified by the certification scheme. The client complies with any requirements that may be prescribed in the certification scheme relating to the use of marks of conformity, and on all product correspondences and product related information. Vista Labs reserves the right to revise or withdraw the requirements as required in order to maintain conformance with FCC rules and regulations governing the product. The product may continue with certification and receive certification upon demonstration of compliance with the revised requirements, to the satisfaction of Vista Laboratories.

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