RESPONSE SUBMISSION REQUIREMENTS Sample Clauses

RESPONSE SUBMISSION REQUIREMENTS. The Respondent shall email one (1) Response in PDF format by the Response Due Date and Time to the E-mail address identified below: Xxxxx Xxxxxxxxx, Contract Analyst County of L.A. - Dept. of Health Services Contracts and Grants Division E-mail: xxxxxxxxxx0@xxx.xxxxxxxx.xxx All Respondents shall provide the name of their Agency and the title and number of the WOS on the subject line. It is the sole responsibility of the submitting Respondent to ensure that its Response is received by the “Response Due Date/Time.” Any Responses received after the “Response Due Date/Time,” as listed in the WOS Timetable, may be eliminated from considered by DHS, at is sole discretion.
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RESPONSE SUBMISSION REQUIREMENTS. The Respondent shall e-mail one (1) Response to the contact person identified in Section 8.0, Contact with County Personnel, by the Response Due Date and Time listed in Section 7.0
RESPONSE SUBMISSION REQUIREMENTS. The Respondent shall email one (1) Response in PDF format by the Response Due Date and Time to the individual identified below: County of Los Angeles - Department of Health Services Contracts and Grants Division Email Address: xxxxx@xxx.xxxxxxxx.xxx All Respondents shall provide the name of their organization and the title and number of the WOS on the subject line. It is the sole responsibility of the submitting Respondent to ensure that its Response is received by the “Response Due Date/Time.” Any Responses received after the “Response Due Date/Time,” as listed in the WOS Timetable, may be eliminated from consideration by DHS, at its sole discretion.
RESPONSE SUBMISSION REQUIREMENTS. Respondents must e-mail one response in PDF format by the response due date and time to the individual identified below: Attn: Xxxx Xxxxx County of Los Angeles, Department of Public Health Email Address: xxxxxx@xx.xxxxxxxx.xxx Respondents must provide the name of their organization and the title and number of this WOS on the subject line of the e-mail. Responses must follow the guidelines as indicated in Exhibit 3, SUBMISSION INSTRUCTIONS. Any deviation from these guidelines will result in the response being disqualified without further review and consideration by DHS, at its sole discretion. Any questions regarding formatting shall be submitted to the individual identified above. It is the sole responsibility of each Respondent to ensure that its response is received by the Response Due Date/Time listed in Section 6.0, above. Any responses received after the Response Due Date/Time listed in Section 6.0, above, may be eliminated from consideration by DHS, at its sole discretion.
RESPONSE SUBMISSION REQUIREMENTS. The Respondent shall e-mail one (1) Response in PDF format by the Response Due Date and Time to the individual identified below: Attn: Xxxxx Xxxxxxxxx, Contract Analyst County of Los Angeles Department of Health Services Contracts and Grants Division E-mail Address: XXxxxxxxxx0@xxx.xxxxxxxx.xxx All Respondents shall provide the name of their organization and the title and number of the WOS on the subject line. It is the sole responsibility of the submitting Respondent to ensure that its Response is received by the “Response Due Date/Time.” Any Responses received after the “Response Due Date/Time,” as listed in the Section 6.0, Work Order Solicitation Timetable, may be eliminated from consideration by DHS at its sole discretion.
RESPONSE SUBMISSION REQUIREMENTS. All questions contained within this section must be answered and all required attachments provided.

Related to RESPONSE SUBMISSION REQUIREMENTS

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

  • 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.

  • Notification Requirement Through and up to the conclusion of the Non-Competition Period, Executive shall give notice to the Company of each new business activity he plans to undertake, at least seven (7) days prior to beginning any such activity. Such notice shall state the name and address of the Person for whom such activity is undertaken and the nature of Executive’s business relationship(s) and position(s) with such Person.

  • 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.‌‌

  • 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.

  • 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.

  • 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.

  • Construction Requirements a) All Life and Safety and applicable Building Codes will be strictly enforced (i.e., tempered glass, fire dampers, exit signs, smoke detectors, alarms, etc.). Prior coordination with the Building Manager is required.

  • Personnel Action Requirements The evaluation procedure contained in this agreement shall not be used in any decision concerning the assignment, reassignment, contract status, non-renewal, termination, reduction or recall of any counselor prior to May 1, 2018.

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