Laboratory Policy definition

Laboratory Policy. The LAB USER agrees to review and abide by all laboratory policies as outlined in the MAF Policies, posted at: xxxxx://xxx.xxxxx.xxxxxxxxxx.xxx/website/wp-content/uploads/2021/03/MAF-user-policies_March-2021.pdf Although MAF provides general safety courses and training on the safe use of specific equipment and processes, the LAB USER assumes responsibility to plan and perform work in such a way as to ensure his/her own personal safety as well as the safety of others in the Facility.
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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. A listing of the current fees can be found at: • xxxxx://xxx.xxxxx.xxxxxxxxxx.xxx/facilities/molecular-analysis-facility/rates/ Any future fee changes in excess of 10% will be made with at least 90 days’ notice. The INSTITUTION is responsible for promptly notifying the MAF facility operations manager in writing if a REMOTE USER ceases to be a student, or employee of, or under contract to the INSTITUTION and is responsible for all fees and costs by such REMOTE USER until such time as the notice is received by the MAF Associate Director. Non-payment of fees within sixty (60) days of receipt of invoice by the INSTITUTION will subject the INSTITUTION to termination of laboratory access with ten (10) days notice to the INSTITUTION. Finance charges at a periodic rate of 1% per month or 12...
Sample 1
Laboratory Policy. The LAB USER agrees to review and abide by all laboratory policies as outlined in: • the MAF Policies, posted at xxxx://xxx.xxxxx.xxxxxxxxxx.xxx/maf/access/userpolicies/ Although MAF provides general safety courses and training on the safe use of specific equipment and processes, the LAB USER assumes responsibility to plan and perform work in such a way as to ensure his/her own personal safety as well as the safety of others in the Facility. 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: • MAF tools: xxxx://xxx.xxxxx.xxxxxxxxxx.xxx/maf/access/ Any future fee changes in excess of 10% will be made with at least 90 days’ notice. The FACULTY USER is responsible for promptly notifying the MAF joint facility operations manager (Xxxxxx Xx, xxxxxxxx@xx.xxx) if a LAB USER ceases to be a student or employee of UW and is responsible for all fees and costs by such LAB USER until such time as written notice is received by the facility operations manager. Non-payment of fees within sixty (60) days of receipt of invoice will subject the LAB USER and the FACULTY USER to termination of laboratory access with ten (10) days notice to the FACULTY USER.
Sample 1

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.

  • Read and agreed: Company (“User”) Acknowledged: Stanford Nanofabrication Facilities (SNF) Authorized Signature Print Name Authorized Signature Xxxx Xxxx Managing Director Title Date Date EXHIBIT B CENTER SPECIFIC PROVISIONS • 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.

  • Read and agreed: Acknowledged: Company: Stanford Nano Shared Facilities (SNSF) Signature: Print Name: Xxxxxx Xxxxx Title: Associate Director, SNSF Date: Date: EXHIBIT B CENTER SPECIFIC PROVISIONS • Laboratory Policy: The USER and USER PERSONNEL agree to abide by all laboratory policies as stated in the SNSF User Personnel Orientation and Safety Manuals, in particular: Safety Responsibility, Respectful Workplace, and Stanford Computer Use and Network Policy.

  • 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.

  • USER SIGNATURE: PRINT NAME: FACULTY/SUPERVISOR SIGNATURE: PRINT NAME: (IF STUDENT IS USER) INSTITUTION NAME: DATE: Exhibit B Service Center Specific Provisions Stanford Nanofabrication Facility 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.

  • 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.

  • Read and agreed: Acknowledged: Institution: Stanford Nano Shared Facilities (SNSF) Signature: Print Name: Xxxxxx Xxxxx Title: Associate Director, SNSF Date: Date: EXHIBIT B CENTER SPECIFIC PROVISIONS  Laboratory Policy: The USER and USER PERSONNEL agree to abide by all laboratory policies as stated in the SNSF User Personnel Orientation and Safety Manuals, in particular: Safety Responsibility, Respectful Workplace, and Stanford Computer Use and Network Policy.

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


More Definitions of Laboratory Policy

Laboratory Policy. The LAB USER agrees to abide by all laboratory policies as outlined in: • the WNF user manual, posted at: xxxx://xxx.xxx.xx.xxx/docs/labusermanual.pdf • the NTUF Policies, posted at: xxxx://xxxxx.xxxxxxxxxx.xxx/ntuf/ Although the WNF and MAF provide general safety courses and training on the safe use of specific equipment, the LAB USER assumes responsibility to plan and perform work in such a way as to ensure his/her own personal safety as well as the safety of others in the Facility.
Sample 1

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).

  • 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 applicable then-current standards for laboratory activities for pharmaceuticals (including biologicals) or vaccines, as applicable, as set forth in the Act and any regulations or guidance documents promulgated thereunder, as amended from time to time, together with any similar standards of good laboratory practice as are required by any Regulatory Authority having jurisdiction over the applicable activity.

  • Participating Clinical Laboratory means a Clinical Laboratory which has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • Quality Management System means a set of interrelated or interacting elements that organisations use to direct and control how quality policies are implemented and quality objectives are achieved;

  • Laboratory or “LANL” means the geographical location of Los Alamos National Laboratory, a federally funded research and development center owned by the DOE / NNSA.

  • Substance Abuse Professional (SAP) means a qualified person who evaluates employees who have violated a DOT drug and alcohol regulation and makes recommendations concerning education, treatment, follow-up testing, and aftercare.

  • Clinical laboratory means a facility for the microbiological, serological, chemical, hematological, radiobioassay, cytological, immunohematological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of a disease or assessment of a medical condition.

  • Quality Assurance Program means the overall quality program and associated activities including the Department’s Quality Assurance, Design-Builder Quality Control, the Contract’s quality requirements for design and construction to assure compliance with Department Specifications and procedures.

  • Non-Participating Clinical Laboratory means a Clinical Laboratory which does not have a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan provide services to you at the time services are rendered.

  • Medical Specialist means any medical practitioner who is vocationally registered by the Medical Council under the Health Practitioners Competence Assurance Act 2003 in one of the approved branches of medicine and who is employed in either that branch of medicine or in a similar capacity with minimal oversight.

  • New Jersey Stormwater Best Management Practices (BMP) Manual or “BMP Manual” means the manual maintained by the Department providing, in part, design specifications, removal rates, calculation methods, and soil testing procedures approved by the Department as being capable of contributing to the achievement of the stormwater management standards specified in this chapter. The BMP Manual is periodically amended by the Department as necessary to provide design specifications on additional best management practices and new information on already included practices reflecting the best available current information regarding the particular practice and the Department’s determination as to the ability of that best management practice to contribute to compliance with the standards contained in this chapter. Alternative stormwater management measures, removal rates, or calculation methods may be utilized, subject to any limitations specified in this chapter, provided the design engineer demonstrates to the municipality, in accordance with Section IV.F. of this ordinance and N.J.A.C. 7:8-5.2(g), that the proposed measure and its design will contribute to achievement of the design and performance standards established by this chapter.

  • Approved laboratory means a laboratory that is listed in the national conference of interstate milk shipments list of sanitation compliance and enforcement ratings distributed by the United States food and drug administration and as approved by the director.

  • Good Manufacturing Practices or “GMP” shall mean the then current Good Manufacturing Practices as such term is defined from time to time by the FDA or other relevant Governmental Authority having jurisdiction over the development, manufacture or sale of the Product in the Territory pursuant to its regulations, guidelines or otherwise.

  • Alcohol abuse means any pattern of pathological use of alcohol that causes impairment in social or occupational functioning, or that produces physiological dependency evidenced by physical tolerance or by physical symptoms when it is withdrawn.

  • Drug Free Workplace Act Party will assure a drug-free workplace in accordance with 45 CFR Part 76. Lobbying: No federal funds under this agreement may be used to influence or attempt to influence an officer or employee of any agency, a member of Congress, an officer or employee of Congress, or an employee of a member of Congress in connection with the awarding of any federal contract, continuation, renewal, amendments other than federal appropriated funds.

  • Quality system means documented organizational procedures and policies: internal audits of those policies and procedures: management review and recommendation for quality improvement.”

  • Project Management Plan means the management plan that (i) sets out a high level workplan to describe the manner in which the Design-Builder will manage the Project, including to address related matters such as traffic management and communications, and (ii) is prepared by or for the Design-Builder and submitted to the Owner;

  • Current Good Manufacturing Practices or “cGMP” means applicable Good Manufacturing Practices as specified in the United States Code of Federal Regulations and/or the EU Good Manufacturing Guidelines, and any successor legislation from time to time, prevailing at the time of the manufacture of the Product.

  • Standards Board means the Professional Standards Board established pursuant to 14 Del.C. §1201.

  • Post-consumer material means a material or finished product that has served its intended use and has been discarded for disposal or recovery, having completed its life as a consumer item. Post consumer material is a part of the broader category of "recycled content."

  • Pest Management Plan and “PMP” means the Recipient’s plan dated March 9, 2010, which: (i) addresses the concerns relating to the Project risks associated with potential increases in the use of pesticides for agricultural production, intensification and diversification and controlling disease vector populations arising from irrigation schemes; (ii) sets forth mitigation and monitoring measures to be taken during Project implementation and operation to eliminate adverse environmental and social impacts, offset them, or reduce them to acceptable levels; (iii) recommends institutional measures to strengthen national capacities to implement the mitigation and monitoring measures; and (iv) as part of the implementation arrangements, identifies national agencies and other partners that could play a vital role in the success of the Project.

  • Procurement Plan means the Recipient’s procurement plan for the Project, dated April 2, 2010, and referred to in paragraph 1.16 of the Procurement Guidelines and paragraph 1.24 of the Consultant Guidelines, as the same shall be updated from time to time in accordance with the provisions of said paragraphs.

  • Procurement Policy means ADB’s Procurement Policy - Goods, Works, Nonconsulting and Consulting Services (2017, as amended from time to time);

  • Stormwater management plan means the set of drawings and other documents that comprise all the information and specifications for the programs, drainage systems, structures, BMPs, concepts and techniques intended to maintain or restore quality and quantity of stormwater runoff to pre-development levels.

  • Web Site Accessibility Standards/Specifications means standards contained in Title 1 Texas Administrative Code Chapter 206.