Laboratory Responsibilities Sample Clauses

Laboratory Responsibilities. The laboratories assigned with responsibility for chemical analyses of environmental media and toxicity testing may include a combination of the following; ■ Pace Analytical Services, Green Bay and Xxxxxxxx, Wisconsin ■ Test America, Dayton, Ohio; ■ Columbia Analytical Services, Kelso, Washington; ■ Xxxxx-Hole Group, Raynham, Massachusetts; ■ New Age/Landmark, Inc., Benton Harbor, Michigan; and ■ Aquatec Biological Sciences, Williston, Vermont. ■ STAT Analysis Corporation, Chicago, Illinois ■ Microbac Laboratories, Inc., Merrillville, Indiana ■ TriMatrix Laboratories, Inc., Grand Rapids, Michigan The laboratories are certified as provided in Appendix A. The laboratory QAMs and State/Federal certifications are also provided in Appendix A. Table 1 in Appendix A summarizes the analyses that each laboratory may be selected to perform. Analytical laboratories will be selected on a site-specific basis based on the following criteria: ■ Laboratory’s ability to accommodate the site-specific schedule; ■ Maintaining consistency with previously performed analysis, particularly with on-going groundwater monitoring; ■ Laboratory costs for analysis; and ■ Laboratory’s experience analyzing select parameters and certification status. The laboratories assigned with responsibility for geotechnical analyses of site media may include a combination of the following: ■ Gestra Engineering Inc. (Gestra), Oak Creek, Wisconsin; ■ Xxxxxx Engineering and Scientists (Xxxxxx), Sheboygan, Wisconsin; and ■ Others, if qualifications are submitted and approved by USEPA. Qualifications and procedures for geotechnical laboratories are provided in Appendix A6 through Appendix A8. Test procedures, described in Appendix A6 and Appendix A7, are only to be used for geotechnical analysis and will not be used for environmental samples. In general, laboratory support will include the following or similar positions: Laboratory Client Services Manager The laboratory Client Services Manager is responsible for the management of the analytical requirements for sample analysis and will interface directly with the Study Leader. The Client Services Manager provides a complete interface with clients from initial project specification to final deliverables.
AutoNDA by SimpleDocs
Laboratory Responsibilities. Initial identification of treatment train options; summarization of results; consultation during design, construction, and startup/testing phases Cooperator Responsibilities: Review and guidance on treatment train options; engineering design, construction, and system testing Resources National Exposure Research Laboratory (NERL) The Laboratory “National Exposure Research Laboratory” (NERL) will contribute technical assistance, logistical support, and analysis of samples. This will include use of EPA facilities, supplies, equipment, and personnel. XYZ Foods, Inc. The Cooperator “XYZ Foods” will provide samples for analysis at EPA facilities. The Cooperator will also contribute data, technical assistance, and supporting research (including use of facilities, personnel and supplies), as needed.
Laboratory Responsibilities 

Related to Laboratory Responsibilities

  • Regulatory Responsibilities The Parties will share responsibility for leading regulatory matters relating to the SYNGAP1 Co-Co Products, as described in this Section 6.9 (each Party, when designated as provided herein to provide such leadership with respect to designated activities is the “Lead Regulatory Party” with respect to such activities). With respect to each SYNGAP1 Co-Co Product, Acadia shall (x) lead the overall strategy for obtaining Regulatory Approval of such SYNGAP1 Co-Co Product (including labeling for such SYNGAP1 Co-Co Product), including by selecting the jurisdictions within which XXXx will be pursued and Execution Version the timing and order in which such approvals will be sought (“Regulatory Strategy”), and will be the Lead Regulatory Party with respect to such strategic activities with respect to such SYNGAP1 Co-Co Product, (y) be the Lead Regulatory Party with respect to the submission of any MAA for such SYNGAP1 Co-Co Product, and (z) following the first Regulatory Approval of such SYNGAP1 Co-Co Product, be the Lead Regulatory Party in connection with such SYNGAP1 Co-Co Product and with respect to Commercialization and regulatory activities (including post-marketing studies). Subject to the foregoing, the JSC shall designate a Party to lead all other pre-Regulatory Approval regulatory matters relating to each SYNGAP1 Co-Co Product in accordance with the applicable SYNGAP1 Co-Development Plan (each Party in such capacity will be deemed the Lead Regulatory Party with respect to such activities). The Lead Regulatory Party shall be responsible for (i) filing for in its name, and owning, all Regulatory Materials relating to regulatory activities with respect to such SYNGAP1 Co-Co Product in the relevant country, (ii) overseeing, monitoring, and coordinating all regulatory actions, communications and filings with, and submissions to, each Regulatory Authority with respect to such activities; and (iii) interfacing, corresponding, and meeting with each Regulatory Authority with respect to such activities, in each case consistent with the Regulatory Strategy and applicable SYNGAP1 Co-Development Plan or SYNGAP1 Co-Commercialization Plan.

  • Regulatory Responsibility The preparation, filing, prosecution and maintenance of INDs, BLAs and other regulatory filings required to be filed with any Regulatory Authority with regard to each Product will be in the name of and the responsibility of Alexion. Alexion shall own the Regulatory Approvals. The costs incurred by the Parties in the preparation, filing and submission of such regulatory filings will be deemed Development Expenses and subject to the terms of Section 3.6. Except as otherwise provided in an applicable Development Plan, Alexion shall oversee, monitor and coordinate all regulatory actions, communications and filings with and submissions, including filings and submissions of supplements and amendments thereto, to Regulatory Authorities with respect to each Product and shall give XOMA a reasonable opportunity for prior review of all such material communications, filings and submissions.

  • ALPS’ Responsibilities In connection with its performance of TA Web, ALPS shall:

  • Specific Responsibilities In addition to its overall responsibility for monitoring and providing a forum to discuss and coordinate the Parties’ activities under this Agreement, the JSC shall in particular:

  • Joint Responsibilities 2.1.1 University and Affiliate each will identify, and notify each other of, a person responsible for serving as its liaison during the course of this affiliation. The appointment of liaisons shall be subject to mutual approval of the parties.

  • Company Responsibilities The Company will undertake responsibilities as set forth below:

  • Monitoring Responsibilities The Custodian shall furnish annually to the Fund, during the month of June, information concerning the foreign sub-custodians employed by the Custodian. Such information shall be similar in kind and scope to that furnished to the Fund in connection with the initial approval of this Contract. In addition, the Custodian will promptly inform the Fund in the event that the Custodian learns of a material adverse change in the financial condition of a foreign sub-custodian or any material loss of the assets of the Fund or in the case of any foreign sub-custodian not the subject of an exemptive order from the Securities and Exchange Commission is notified by such foreign sub-custodian that there appears to be a substantial likelihood that its shareholders' equity will decline below $200 million (U.S. dollars or the equivalent thereof) or that its shareholders' equity has declined below $200 million (in each case computed in accordance with generally accepted U.S. accounting principles).

  • Development Responsibilities Unless the Parties agree in writing upon an alternate allocation of responsibility, the Parties shall have the following rights and obligations with respect to operational responsibilities under each Development Plan:

  • Client Responsibilities You are responsible for (a) assessing each participants’ suitability for the Training, (b) enrollment in the appropriate course(s) and (c) your participants’ attendance at scheduled courses.

  • Contractor Responsibilities 19.1. Contractor shall perform national criminal history checks for Ohio, Indiana, and Kentucky, and 10-panel drug screening tests on all prospective employees performing work under this RFP or coming onto a CMHA property and any resulting contract and provide summaries of the results to the Authority if requested. For the purposes of this section, the term “employees” includes contractor. Prospective employees whose criminal background check discloses a misdemeanor or felony involving crimes of moral turpitude, sexual offenses or harm to persons or property shall not be employed to perform work under this RFP or any resulting contract. Contractor is required to perform drug screening of all employees and to ensure acceptable test results. Criminal history and drug screening checks will be completed at the sole expense of the contractor. Any employee of the Contractor suspected of being under the influence of drugs and or alcohol will be reported to the appropriate personnel at CMHA and/or other local law enforcement. If the employee is determined to be under the influence of drugs or alcohol in any form or manner, or believed by proper authority to be dealing in illicit sale of alcohol or drugs they will be removed and shall not be allowed to return to any job site on the Authority’s property. The Contractor’s contract may be suspended and/or terminated should such a situation occur or if the Contractor fails to submit results pursuant to this section.

Time is Money Join Law Insider Premium to draft better contracts faster.