Minimum Technology Guidelines Sample Clauses

Minimum Technology Guidelines. CFI recognizes that Region 4 will, at its discretion, adopt minimum technology guidelines and the Courts will at a minimum, provide equipment that meets those guidelines. Once the Region adopts minimum technology guidelines, it will provide CFI with 90 days’ advance written notice and upon request from CFI, it will meet and confer regarding the impact of the decision to adopt minimum technology guidelines. On a Court-by- Court basis, the Region will provide to CFI a demonstration of a VRI event using the selected technology prior to implementation of its decision on technology. 1. VRI Guidelines a. In addition to the guidelines set forth below in the text of this MOU, the Region adopts the attached JCC Guidelines for VRI for spoken language interpreting events as an addendum to this MOU. Where or if the JCC guidelines are determined to conflict with the guidelines below, the guidelines in Section II shall prevail. b. When a home court interpreter is not available within the home court county an individual analysis should be made of the language and legal demands of the case before recommending VRI. The interpreter coordinator/manager should perform this analysis. This analysis should consider whether the use of VRI is appropriate based on the following guidelines: i. Events that are expected to last less than 30 minutes in duration. ii. Events that are not complex, and are generally non- evidentiary. iii. Events involving uncontested infractions that require no testimony, like traffic cases. iv. Events of a nature that cannot be delayed such as arraignments for in–custody defendants, bond review hearings, bail reductions, and temporary restraining orders. v. Out-of-court communications involving interviews such as attorney-client conference, self-help centers, post-court services, review of probation conditions, pre-trial services and inquiries from the public. c. Training: prior to implementing VRI, training will be provided to Judicial Officers, interpreters and court staff on the use of these guidelines, checklist, as well as the use of the court’s VRI equipment, including but not limited to, an explanation and demonstration as to how the equipment works.
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Minimum Technology Guidelines. CFI recognizes that Region 3 will, at its discretion, adopt minimum technology guidelines and the Courts will, at a minimum, provide equipment that meets those guidelines. 1. Compensation – Interpreters who are assigned to perform spoken language VRI shall receive a 25% stipend for any day in which they perform spoken language VRI. The stipend for part-time interpreters shall be based upon the number of hours they were assigned to work on that day.

Related to Minimum Technology Guidelines

  • Technology Research Analyst Job# 1810 General Characteristics

  • HIV/AIDS Model Workplace Guidelines Grantee will: a. implement the System Agency’s policies based on the Human Immunodeficiency Virus/Acquired Immunodeficiency Syndrome (HIV/AIDS), AIDS Model Workplace Guidelines for Businesses at xxxx://xxx.xxxx.xxxxx.xx.xx/hivstd/policy/policies.shtm, State Agencies and State Grantees Policy No. 090.021. b. educate employees and clients concerning HIV and its related conditions, including AIDS, in accordance with the Texas. Health & Safety Code §§ 85.112-114.

  • Clinical Data and Regulatory Compliance The preclinical tests and clinical trials, and other studies (collectively, “studies”) that are described in, or the results of which are referred to in, the Registration Statement or the Prospectus were and, if still pending, are being conducted in all material respects in accordance with the protocols, procedures and controls designed and approved for such studies and with standard medical and scientific research procedures; each description of the results of such studies is accurate and complete in all material respects and fairly presents the data derived from such studies, and the Company and its subsidiaries have no knowledge of any other studies the results of which are inconsistent with, or otherwise call into question, the results described or referred to in the Registration Statement or the Prospectus; the Company and its subsidiaries have made all such filings and obtained all such approvals as may be required by the Food and Drug Administration of the U.S. Department of Health and Human Services or any committee thereof or from any other U.S. or foreign government or drug or medical device regulatory agency, or health care facility Institutional Review Board (collectively, the “Regulatory Agencies”); neither the Company nor any of its subsidiaries has received any notice of, or correspondence from, any Regulatory Agency requiring the termination, suspension or modification of any clinical trials that are described or referred to in the Registration Statement or the Prospectus; and the Company and its subsidiaries have each operated and currently are in compliance in all material respects with all applicable rules, regulations and policies of the Regulatory Agencies.

  • Research Use Reporting To assure adherence to NIH GDS Policy, the PI agrees to provide annual Progress Updates as part of the annual Project Renewal or Project Close-out processes, prior to the expiration of the one (1) year data access period. The PI who is seeking Renewal or Close-out of a project agree to complete the appropriate online forms and provide specific information such as how the data have been used, including publications or presentations that resulted from the use of the requested dataset(s), a summary of any plans for future research use (if the PI is seeking renewal), any violations of the terms of access described within this Agreement and the implemented remediation, and information on any downstream intellectual property generated from the data. The PI also may include general comments regarding suggestions for improving the data access process in general. Information provided in the progress updates helps NIH evaluate program activities and may be considered by the NIH GDS governance committees as part of NIH’s effort to provide ongoing stewardship of data sharing activities subject to the NIH GDS Policy.

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  • Development Standards For any structure built on the Property following the Effective Date, it shall comply with the requirements contained in Exhibit B, “Building Materials,” attached hereto and incorporated herein. The Parties agree and acknowledge that the provisions of this Paragraph shall apply to any structure constructed subsequent to the execution of this Agreement. Nothing in this Agreement shall be deemed to modify or otherwise amend any zoning regulation duly adopted by the Town, previously or in the future.

  • Protocols Each party hereby agrees that the inclusion of additional protocols may be required to make this Agreement specific. All such protocols shall be negotiated, determined and agreed upon by both parties hereto.

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  • Hot Weather Guidelines For the purposes of site based discussions regarding the need to plan and perform work during expected periods of hot weather, the following issues shall be considered in conjunction with proper consideration of Occupational Health and Safety issues.

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