Laboratory Director Clause Samples

Laboratory Director. The Practice shall appoint one of its Practice Providers who is a licensed pathologist to serve as the laboratory director (the “Laboratory Director”) of the laboratory operated by , an affiliate of Manager. The Laboratory Director shall maintain the Practice’s standards and professional ethics and those of the medical profession. The duties of the Laboratory Director shall include, but shall not be limited to, monitoring testing results, evaluating quality controls and implementing corrective actions in conjunction therewith; reviewing procedure manuals, including amendments thereto; reviewing policies regarding specimen repeat and slide review ranges; assisting in the provision of continuing education for technologists; acting as a liaison between Manager and physicians and other laboratories; and performing such other duties as are required of a laboratory director under the Clinical Laboratory Improvements Act and other applicable state laws.
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Laboratory Director. With accreditation of Environmental Laboratory Accreditation Program (ELAP), an employee serving as the Laboratory Director shall receive 7% above base pay. The assignment shall be made available on an equal basis to all eligible employees and rotated every two (2) years concurrent with laboratory certification renewal from the State. The following job classifications shall be eligible for this differential pay: Water Treatment Plant Operator Classes Water Treatment Plant Operations Supervisor
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Laboratory Director. The Laboratory Director will be identified in the Site-specific 23 QAPP Addenda. The Laboratory Director is responsible for the following: 24 1. Coordinating the analysis of the samples and selecting the analytical team. 25 2. Coordinating the receipt of the samples at the laboratory. 26 3. Ensuring internal laboratory audits are conducted per the Laboratory’s Quality 27 Assurance Manual (QAM), and distributing the applicable sections of the QAPP 28 and subsequent revisions to members of the analytical team. 29 4. Instituting corrective actions for problems encountered in the chemical analyses 30 and reporting laboratory problems affecting the project data to the Project 31 Manager. Corrective actions for chemical analyses will be detailed in a lab report 32 that will be provided via electronic mail.
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Laboratory Director. Consultant shall provide either (i) two laboratory directors, one of which is licensed to practice medicine without restriction in the State of California, and the other of which holds a certificate of qualification in generic testing/molecular oncology in the State of New York, or (ii) one laboratory director who meets both criteria set forth in the previous clause (i) (such laboratory director(s), the “Laboratory Director(s)”) each of whom will be licensed and qualified, and shall remain in good standing with, all applicable federal and state laws, including, without limit, the federal Clinical Laboratory Improvement Amendments and its implementing regulations (“CLIA”); the State of California’s Business and Professions Code and/or the applicable state laboratory laws and rules in the state of New York, as applicable; the Laboratory’s accrediting bodies (if applicable) (collectively, the “Laboratory Rules”). The Laboratory Directors shall be responsible for performing, or arranging for or delegating as permitted, all the duties and responsibilities required under the Laboratory Rules (the “Laboratory Director Services”). Each Laboratory Director will assist the Laboratory in maintaining compliance with all applicable federal and state laws, rules, regulations, standards and ordinances, and judicial and administrative interpretations thereof, all criteria and standards of applicable accreditation agencies of Laboratory, and all other policies and procedures duly established by Company and the Laboratory, including, without limit, the services and activities set forth in Exhibit A attached hereto. At all times during the term of this Agreement, Laboratory Director will meet all of the qualifications (“Laboratory Director Qualifications”) as follows: (i) Licensed to practice medicine without restriction in the State of California or the State of New York, as applicable; (ii) Eligible and compliant with all criteria for laboratory director of a high complexity laboratory under the Laboratory Rules; (iii) Eligible to enroll and participate in any federal and state government health care programs; and (iv) Compliant with (a) the policies and procedures of Company and the Laboratory and (b) the requirements of various governmental and accrediting agencies applicable to Laboratory, as may be amended from time to time.
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Laboratory Director. Shall meet the Secretary of the Interior’s historic preservation qualification standards for Archaeologist, including a graduate degree in Anthropology with a specialization in Archaeology or a graduate degree in Archaeology or related field as defined in FR Vol. 62 (119): 33707-337231 for archaeologist; OR meet the Secretary of Interior’s historic preservation qualification standards for Conservator, including a graduate degree in Conservation or graduate degree in a closely related field of study with a certificate in Conservation; Plus five (5) years full-time professional experience applying the theories, methods, and practices of Pacific (Micronesia and Polynesia) or Asian archaeology that enables professional judgments to be made about the identification, evaluation, documentation, or treatment of prehistoric or historic archaeological materials in the Pacific or Asia, as appropriate for the assignment, and which includes professional supervisory experience working with various midden, artifact, and other cultural materials from the Pacific and/or Asia. This person(s) shall have products and activities that demonstrate the successful ability to implement research designs, conduct and supervise laboratory analyses, make strategic decision in the laboratory, and communicate orally and in writing as evidenced by their completed technical reports and/or publications. This person(s) shall work closely with the Principal Investigator and Project Director, write all technical laboratory reports, oversee and direct procurement of all analyses, materials processing, cataloging and conservation, data production, and data base management as necessary.
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Laboratory Director. The Laboratory Director is a technical advisor and is responsible for summarizing and reporting overall unit performance. Responsibilities include: ■ Provide technical, operational, and administrative leadership; ■ Allocation and management of personnel and equipment resources; ■ Quality performance of the facility; ■ Certification and accreditation activities; and ■ Compliance with audits and corrective actions.
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Related to Laboratory Director

  • Technical Committee 1. The Technical Committee shall comprise: (a) nine experts representing different regions of the Agreement Area, in accordance with a balanced geographical distribution; (b) one representative from the International Union for Conservation of Nature and Natural Resources (IUCN), one from the International Waterfowl and Wetlands Research Bureau (IWRB) and one from the International Council for Game and Wildlife Conservation (CIC); and (c) one expert from each of the following fields: rural economics, game management, and environmental law. The procedure for the appointment of the experts, the term of their appointment and the procedure for designation of the Chairman of the Technical Committee shall be determined by the Meeting of the Parties. The Chairman may admit a maximum of four observers from specialized international inter- governmental and non-governmental organizations. 2. Unless the Meeting of the Parties decides otherwise, meetings of the Technical Committee shall be convened by the Agreement secretariat in conjunction with each ordinary session of the Meeting of the Parties and at least once between ordinary sessions of the Meeting of the Parties. 3. The Technical Committee shall: (a) provide scientific and technical advice and information to the Meeting of the Parties and, through the Agreement secretariat, to Parties; (b) make recommendations to the Meeting of the Parties concerning the Action Plan, implementation of the Agreement and further research to be carried out; (c) prepare for each ordinary session of the Meeting of the Parties a report on its activities, which shall be submitted to the Agreement secretariat not less than one hundred and twenty days before the session of the Meeting of the Parties, and copies shall be circulated forthwith by the Agreement secretariat to the Parties; and (d) carry out any other tasks referred to it by the Meeting of the Parties. 4. Where in the opinion of the Technical Committee there has arisen an emergency which requires the adoption of immediate measures to avoid deterioration of the conservation status of one or more migratory waterbird species, the Technical Committee may request the Agreement secretariat to convene urgently a meeting of the Parties concerned. These Parties shall meet as soon as possible thereafter to establish rapidly a mechanism to give protection to the species identified as being subject to particularly adverse threat. Where a recommendation has been adopted at such a meeting, the Parties concerned shall inform each other and the Agreement secretariat of measures they have taken to implement it, or of the reasons why the recommendation could not be implemented. 5. The Technical Committee may establish such working groups as may be necessary to deal with specific tasks.

  • Medical Director The Contractor shall employ the services of a Medical Director who is a licensed Indiana Health Care Provider (IHCP) provider board certified in family medicine or internal medicine. If the Medical Director is not board certified in family medicine, they shall be supported by a clinical team with experience in pediatrics, behavioral health, adult medicine and obstetrics/gynecology. The Medical Director shall be dedicated full-time to the Contractor’s Indiana Medicaid product lines. The Medical Director shall oversee the development and implementation of the Contractor’s disease management, case management and care management programs; oversee the development of the Contractor’s clinical practice guidelines; review any potential quality of care problems; oversee the Contractor’s clinical management program and programs that address special needs populations; oversee health screenings; serve as the Contractor’s medical professional interface with the Contractor’s primary medical providers (PMPs) and specialty providers; and direct the Quality Management and Utilization Management programs, including, but not limited to, monitoring, corrective actions and other quality management, utilization management or program integrity activities. The Medical Director, in close coordination with other key staff, is responsible for ensuring that the medical management and quality management components of the Contractor’s operations are in compliance with the terms of the Contract. The Medical Director shall work closely with the Pharmacy Director to ensure compliance with pharmacy-related responsibilities set forth in Section 3.4. The Medical Director shall attend all OMPP quality meetings, including the Quality Strategy Committee meetings. If the Medical Director is unable to attend an OMPP quality meeting, the Medical Director shall designate a representative to take his or her place. Notwithstanding the Medical Director ‘s sending of a representative, the Medical Director shall be responsible for knowing and taking appropriate action on all agenda and action items from all OMPP quality meetings.

  • Laboratory Testing All laboratories selected by UPS Freight for analyzing Controlled Substances Testing will be HHS certified.

  • Project Director The individual designated by the juvenile board or Chief Administrative Officer, who is to be responsible for the administration and coordination of grant funds in accordance with this Contract ,, the general grant requirements, and applicable Targeted Grant requirements.

  • Joint Commercialization Committee Upon a decision by the JSC to activate the joint Commercialization committee, but in no case later than eighteen (18) months prior to the projected First Commercial Sale (the “Joint Commercialization Committee” or “JCC”), the Parties shall establish the JCC. The JCC shall hold its initial meeting within thirty (30) days of its establishment. Following its initial meeting, the JCC will meet in person, by teleconference or by video-teleconference at least [***] per [***] to review and discuss material decisions and key activities that relate to the matters set forth below. The JCC will be responsible for the communication, review and discussion of the Commercialization Plan and other Commercialization matters, including marketing strategy and planning, pricing, commercial manufacture, and [***], in each case in the Territory. Without limiting the foregoing, the JCC shall be responsible for: (a) reviewing and consulting with Coherus on the Commercialization Plan prior to adoption of the Commercialization Plan or changes by Licensee; (b) recommending the Commercialization Plan for approval by the JSC prior to adoption of the Commercialization Plan; (c) communicating with the JDC regarding the interrelationship between Development activities and potential Commercialization activities; (d) reviewing and monitoring the activities and progress against the Commercialization Plan; (e) monitoring and reporting on the competitive landscape for the Product in the Territory; (f) establishing appropriate processes for coordinating review of promotional materials for the Territory to ensure compliance with Applicable Laws and industry best practices; (g) overseeing the trademark and publication strategies for the Territory; and (h) communicating with the Parties regarding all of the foregoing.