Laboratory Coats Clause Samples

The 'Laboratory Coats' clause establishes requirements regarding the provision and use of lab coats within a laboratory setting. Typically, this clause specifies whether the employer or institution is responsible for supplying lab coats to staff, outlines standards for their maintenance and cleanliness, and may address when and where lab coats must be worn. By clearly defining these responsibilities, the clause helps ensure safety, hygiene, and compliance with workplace regulations, while also preventing disputes over who bears the cost or duty of providing protective clothing.
Laboratory Coats. Memorial shall provide Fellow with no less than one
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Laboratory Coats. ‌ The Hospital agrees to continue the present practice with respect to the supply and laundering of laboratory coats. For clarity, cuffed coats with snaps are to be supplied to employees in the Labs.
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Laboratory Coats. Broward Health shall provide Resident with no less than one (1) laboratory coat which is to be worn by Resident while Resident is on duty at a Broward Health Designated Facility. The undersigned hereby acknowledges access to or receipt of Broward Health’s Code of Conduct, Broward Health’s Policies & Procedures, and the Graduate Medical Education’s Programs Policies & Procedures which pertain to, but are not limited to: a. Evaluation of Resident’s performance in the Residency Program, including but not limited to provisions for promotion, demotion, reappointment, retention and dismissal; b. Moonlighting;
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Laboratory Coats. The District agrees to provide employees with three laboratory coats to wear while working and to provide laundering services for such coats.
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Laboratory Coats. Memorial shall provide Resident with no less than one
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Laboratory Coats. Broward Health shall provide Resident with no less than one (1) laboratory coat which is to be worn by Resident while Resident is on duty at a Broward Health Designated Facility. The undersigned hereby acknowledges access to or receipt of the following: 1. Broward Health Policies & Procedures Manual. 2. Broward Health, Office of Graduate Medical Education Policies & Procedures Manual. 3. Broward Health Code of Conduct.
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Related to Laboratory Coats

  • Laboratory a. Drug tests shall be conducted by laboratories licensed and approved by SAMSHA which comply with the American Occupational Medical Association (AOMA) ethical standards. Upon advance notice, the parties retain the right to inspect the laboratory to determine conformity with the standards described in this policy. The laboratory will only test for drugs identified in this policy. The City shall bear the cost of all required testing unless otherwise specified herein. b. Tests for all controlled substances, except alcohol, shall be by oral fluid testing and shall consist of two procedures, a screen test and, if that is positive, a confirmation test. c. To be considered positive for reporting by the laboratory to the City, both samples must be tested separately in separate batches and must also show positive results on the confirmatory test. d. In the event of a positive test, the testing laboratory will perform an automatic confirmation test on the original specimen at no cost to the Covered Employee. In addition, the testing laboratory shall preserve a sufficient specimen to permit an independent re-testing at the Covered Employee’s request and expense. The same, or any other, approved laboratory may conduct re-tests. The laboratory shall endeavor to notify the designated MRO of positive drug, alcohol, or adulterant tests results within five (5) working days after receipt of the specimen.

  • Laboratory Services Covered Services include prescribed diagnostic clinical and anatomic pathological laboratory services and materials when authorized by a Member's PCP and HPN’s Managed Care Program.

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

  • Manufacturing (a) The Supplier shall without limitation be responsible, at no additional cost to the Purchaser, for: sourcing and procuring all raw materials for the Products; obtaining all necessary approvals, permits and licenses for the manufacturing of the Products; providing sufficient qualified staff and workers to perform the obligations under this Purchase Agreement; implementing and maintaining effective inventory and production control procedures with respect to the Products; and handling other matters as reasonably requested by the Purchaser from time to time. (b) The Supplier shall not change any process, material, component, packaging or manufacturing location without the Purchaser’s express prior written approval.

  • Research Use The Requester agrees that if access is approved, (1) the PI named in the DAR and (2) those named in the “Senior/Key Person Profile” section of the DAR, including the Information Technology Director and any trainee, employee, or contractor1 working on the proposed research project under the direct oversight of these individuals, shall become Approved Users of the requested dataset(s). Research use will occur solely in connection with the approved research project described in the DAR, which includes a 1-2 paragraph description of the proposed research (i.e., a Research Use Statement). Investigators interested in using Cloud Computing for data storage and analysis must request permission to use Cloud Computing in the DAR and identify the Cloud Service Provider (CSP) or providers and/or Private Cloud System (PCS) that they propose to use. They must also submit a Cloud Computing Use Statement as part of the DAR that describes the type of service and how it will be used to carry out the proposed research as described in the Research Use Statement. If the Approved Users plan to collaborate with investigators outside the Requester, the investigators at each external site must submit an independent DAR using the same project title and Research Use Statement, and if using the cloud, Cloud Computing Use Statement. New uses of these data outside those described in the DAR will require submission of a new DAR; modifications to the research project will require submission of an amendment to this application (e.g., adding or deleting Requester Collaborators from the Requester, adding datasets to an approved project). Access to the requested dataset(s) is granted for a period of one (1) year, with the option to renew access or close-out a project at the end of that year. Submitting Investigator(s), or their collaborators, who provided the data or samples used to generate controlled-access datasets subject to the NIH GDS Policy and who have Institutional Review Board (IRB) approval and who meet any other study specific terms of access, are exempt from the limitation on the scope of the research use as defined in the DAR.