Laboratory Policy definition

Laboratory Policy. The LAB USER agrees to abide by all laboratory policies as outlined in:
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Laboratory Policy. The REMOTE USER agrees to provide a sufficiently detailed description of services and characterization needs required for completion of remote services. In addition, the REMOTE USER is responsible for any measures required to transport and secure the samples (e.g., International Traffic in Arms Regulations (ITAR) or Export Administration Regulation controls), as well as specifying the environmental control and storage conditions for the samples. MAF Staff will perform the remote services on a fee for services basis using a best effort, time and materials cost reimbursement delivery model. MAF Staff will utilize best available business practices, process methodologies, and materials selections prior to committing technical samples to the work stream. Remote services will be completed in as timely a manner as possible, but may be impacted by equipment and process engineering availability. Upon entering the work stream, the lead MAF Staff member will provide the REMOTE USER with an initial schedule and will send notifications of any events that may result in significant deviation from the schedule. Fees: Upon initiation of a remote services request, the lead MAF Staff member will furnish the REMOTE USER with a good-faith estimate of lab fees, labor hours, materials, and other purchases required to complete the remote services. The INSTITUTION acknowledges responsibility for purchases, materials costs and lab fees incurred by the REMOTE USER in his/her use of the MAF. The lead MAF Staff member will notify the REMOTE USER of any expenditure that will result in exceeding a 10% variance above the good-faith estimate and halt remote services until the REMOTE USER approves the variance.
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Laboratory Policy. The LAB USER agrees to review and abide by all laboratory policies as outlined in the MAF Policies, posted at:
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Examples of Laboratory Policy in a sentence

  • Routine biochemistry and hematology test results will be reported to the EMR, in conformance with the times published in the Laboratory Policy Manual.

  • Except where clearly inconsistent with an express provision of this contract, the provisions of Laboratory Policy applicable to nonbargaining unit wage employees of the Laboratory shall be applicable to the Em- ployees.

  • It does not include the withholding or granting of any wage adjustments or any question of interpretation of Laboratory Policy.

  • Laboratory Policy: The LAB-USER agrees to abide by all laboratory policies, as stated in the RIT Semiconductor Nanofabrication Laboratory (SNL) Lab-User Orientation and Safety training and in manuals posted throughout the laboratory.

  • Authorized Signature Authorized Signature ▇▇▇▇ ▇▇▇▇ (SNF) / ▇▇▇▇▇▇ ▇▇▇▇▇ (SNSF) Print Name Managing Director Title • Laboratory Policy: The User and User Personnel agree to abide by all laboratory policies as stated in the SNF/SNSF User Personnel Orientation and Safety Manuals, in particular: Safety Responsibility, Respectful Workplace, and Stanford Computer Use and Network Policy.

  • Company (“User”) Stanford Nanofabrication Facilities (SNF) Authorized Signature ▇▇▇▇ ▇▇▇▇ Managing Director Title • Laboratory Policy: The User and User Personnel agree to abide by all laboratory policies as stated in the SNF User Personnel Orientation and Safety Manuals, in particular: Safety Responsibility, Respectful Workplace, and Stanford Computer Use and Network Policy.

  • Administrative Matters Administrative matters, including policy interpretation, and related issues are the responsibility of the following individual offices designated by each agency: N8Q QQE Office of Administration Office of Laboratory Policy Office of Energy Research Representatives of these designated offices will meet as necessary to discuss and resolve any problems or issues which may affect either agency's ability to carry out the provisions of this agreement.


More Definitions of Laboratory Policy

Laboratory Policy. The LAB USER agrees to review and abide by all laboratory policies as outlined in: Fees: The FACULTY USER acknowledges responsibility for purchases, materials costs and lab fees incurred by the LAB USER in his/her use of the MAF. A listing of the current fees can be found at:
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Related to Laboratory Policy

  • Good Laboratory Practices or “GLP” means the then-current good laboratory practice standards promulgated or endorsed by the FDA, as defined in U.S. 21 C.F.R. Part 58 (or such other comparable regulatory standards in jurisdictions outside the United States, as they may be updated from time to time).

  • Quality Management Plan means the portion of the Project Development Plan providing the information requested in Section 4.3 of Exhibit B to the ITP.

  • Drug-free workplace means a site for the performance of work done in connection with a specific contract at which the employees of the Contractor are prohibited from engaging in the unlawful manufacture, distribution, dispensing, possession, or use of a controlled substance.

  • Good Laboratory Practice or “GLP” means the current standards for laboratory activities for pharmaceuticals, as set forth in the FDA’s Good Laboratory Practice regulations or the Good Laboratory Practice principles of the Organization for Economic Co-Operation and Development, as amended from time to time, and such standards of good laboratory practice as are required by the European Union and other organizations and governmental agencies in countries in which a Product is intended to be sold, to the extent such standards are not less stringent than United States Good Laboratory Practice.

  • Professional development plan means a plan specifically designed to identify goals, activities and measurable objectives that will support continuous learning related to professional knowledge, skills and abilities.