DRUG-FREE WORK PLACE definition

DRUG-FREE WORK PLACE means the site(s) for the performance of work done by the Contractor in connection with a specific contract at which employees of the Contractor are prohibited from engaging in the unlawful manufacture, distribution, dispensing, possession, or use of a controlled substance.
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DRUG-FREE WORK PLACE. PREFERENCE
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DRUG-FREE WORK PLACE. VIM represents it maintains a drug free workplace policy. As a result of this existing policy, VIM agrees to advise its employees and the employees of its subcontractors and agents (hereinafter for the purposes of this provision collectively referred to as "VIM employees"), that: (i) it is the policy of *** that the use, possession, sale, transfer, or purchase of illegal drugs on the *** Oro Grande Property, is prohibited; (ii) entry onto the *** Oro Grande Property constitutes the presence of an employee's vehicle on the *** Oro Grande Property and/or any personal effects of an employee which the employee brings with him or her while entering, on or leaving the *** Oro Grande Property; and (iii) any employee who is found in violation of the policy or who refuses to permit an inspection by an authorized representative of *** may be removed and barred from the *** Oro Grande Property, at the discretion of ***.
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Examples of DRUG-FREE WORK PLACE in a sentence

  • Preparer’s Name Date Authorizing Agent Date NOTE: This document must be signed and included with your BidFORM 00450 DRUG-FREE WORK PLACE Drug-Free Work Place: Yes N/A If yes please complete the form.

  • DRUG-FREE WORK PLACE CERTIFICATE IDENTICAL TIE BIDS - Pursuant to Section 287.087, Florida Statutes, preference shall be given to business with Drug-Free Work Place Programs.

  • DRUG-FREE WORK PLACE The Drug-Free Workplace Act of 1988, found at Title 5, Subtitle D, Anti-Drug Abuse Act of 1988, Public Law No. 100-690 (DFWA), requires grantees of federal agencies to certify that they will provide a drug-free workplace.

  • DRUG-FREE WORK PLACE The bidder/proposer certifies that s/he will provide a drug-free work place by: A.

  • COVERDELL DRUG-FREE WORK- PLACE PROGRAM.—Section 27(g)(1) of the Small Business Act (15 U.S.C. 654(g)(1)) is amended by striking ‘‘2001 through 2003’’ and inserting ‘‘2004 through 2006’’.

  • CERTIFICATION OF DRUG-FREE WORK PLACE: Provider certifies and agrees that Provider and its employees shall comply with County’s policy of maintaining a drug-free work place.

  • Preparer’s Name Date Authorizing Agent Date NOTE: This document must be signed and included with your Bid FORM 00450 DRUG-FREE WORK PLACE Drug-Free Work Place: Yes N/A If yes please complete the form.

  • COVERDELL DRUG-FREE WORK- PLACE PROGRAM.—Section 27 of the Small Business Act (15 U.S.C. 654) is repealed.

  • DRUG-FREE WORK PLACE Contractor acknowledges that the Government maintains a drug free work place in compliance with Drug-Free Workplace Act of 1988 (Pub.

  • Signature Date Printed NameFORM 00450 DRUG-FREE WORK PLACE Drug-Free Work Place: Yes N/A If yes, please complete the form.


More Definitions of DRUG-FREE WORK PLACE

DRUG-FREE WORK PLACE means a site for the performance of work done in connection with a specific grant or contract at which employees are prohibited from engaging in the unlawful manufacture, distribution, dispensing, possession, or use of a controlled substance.
Sample 1
DRUG-FREE WORK PLACE means a site for the performance of work at which employees are prohibited from engaging in the unlawful possession, use, manufacture, distribution, or dispensing of a controlled substance. Work Place shall include residences, apartments, school, offices, parking lots, grounds, sidewalks, access roadways, garages, common lobbies, or hallways or other similar areas.
Sample 1
DRUG-FREE WORK PLACE. VIM represents it maintains a drug free workplace policy. As a result of this existing policy, VIM agrees to advise its employees and the employees of its subcontractors and agents (hereinafter for the purposes of this provision collectively referred to as “VIM employees”), that: (i) it is the policy of Riverside that the use, possession, sale, transfer, or purchase of illegal drugs on the Riverside Oro Grande Property, is prohibited; (ii) entry onto the Riverside Oro Grande Property constitutes the presence of an employee’s vehicle on the Riverside Oro Grande Property and/or any personal effects of an employee which the employee brings with him or her while entering, on or leaving the Riverside Oro Grande Property; and (iii) any employee who is found in violation of the policy or who refuses to permit an inspection by an authorized representative of Riverside may be removed and barred from the Riverside Oro Grande Property, at the discretion of Riverside.
Sample 1

Related to DRUG-FREE WORK PLACE

  • 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.

  • Site / Work place means the lands and other spaces above & below the ground level on which the works are to be carried out, any other lands or places provided by the Owner for the purpose of the Contract.

  • Large work place means a place at which, at an average 500 or more workers are employed in connection with construction work.

  • Drug Free Workplace Act Party will assure a drug-free workplace in accordance with 45 CFR Part 76.

  • Work place means a place at which, at an average 20 or more workers are employed in connection with construction work.

  • Additional SDU Study means a deliverability study that a Developer may elect to pursue as that term is defined in OATT Section 25 (OATT Attachment S). For purposes of Section 23.4.5 of this Attachment H, “Affiliated Entity” shall mean, with respect to a person or Entity:

  • Alcohol Screening Device (ASD) means a breath or saliva device, other than an Evidential Breath Testing Device (EBT), that is approved by the National Highway Traffic Safety Administration and placed on its Conforming Products List for such devices.

  • Project Specific IPRs means: (a) IPRs in the Services provided by the Supplier (or by a third party on behalf of the Supplier) specifically for the purposes of the Contract and all updates and amendments of these items created during the Contract Period; and/or (b) IPRs arising as a result of the provision of the Services by the Supplier (or by a third party on behalf of the Supplier) under the Contract, [including the rights in or to any database developed and supplied by the Supplier to the Customer in accordance with the terms of this Contract;

  • Manufacturing Know-How means all information, techniques, inventions, discoveries, improvements, practices, methods, knowledge, skill, experience and other technology, whether or not patentable or copyrightable, and any copyrights based thereon, relating to or necessary or useful for the production, purification, packaging, storage and transportation of Collaboration Products, including without limitation specifications, acceptance criteria, manufacturing batch records, standard operating procedures, engineering plans, installation, operation and process qualification protocols for equipment, validation records, master files submitted to the FDA, process validation reports, environmental monitoring processes, test data including pharmacological, toxicological and clinical test data, cost data and employee training materials.

  • technical specification means a document that prescribes technical requirements to be fulfilled by a product, process or service;

  • Development Site means any parcel or lot on which exists or which is intended for building development other than the following:

  • Clinical supervisor means any of the following:

  • Project specific information means such part of the Instructions to Consultants used to reflect specific project and assignment conditions.

  • 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.

  • MSAA Indicator Technical Specifications document means, as the context requires, either or both of the document entitled “Multi-Sector Service Accountability Agreement (MSAA) 2019-20 Indicator Technical Specifications November 5, 2018 Version 1.3” and the document entitled “Multi-Sector Service Accountability Agreement (MSAA) 2019-20 Target and Corridor-Setting Guidelines” as they may be amended or replaced from time to time;

  • 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.

  • Commercially Sensitive Information Schedule means the Schedule containing a list of the Commercially Sensitive Information.

  • site development plan means a dimensioned plan drawn to scale that indicates details of the proposed land development, including the site layout, positioning of buildings and structures, property access, building designs and landscaping;

  • Licensed clinical social worker means an individual who meets the licensed clinical social worker requirements established in KRS 335.100.

  • Phase I Clinical Study means a human clinical study of a product, the principal purpose of which is a preliminary determination of safety in healthy individuals or patients, as described in 21 C.F.R. 312.21(a).

  • Manufacturing Materials means parts, tools, dies, jigs, fixtures, plans, drawings, and information produced or acquired, or rights acquired, specifically to fulfill obligations set forth herein.

  • Technical Specifications A specification in a document defining the characteristics of a product or a service, such as the quality levels, the environmental and climate performance levels, the design for all needs, including accessibility for people with disabilities, and the evaluation of conformity, of product performance, of the use of the product, safety or dimensions, as well as requirements applicable to the product as regards the name by which it is sold, terminology, symbols, testing and test methods, packaging, marking or labelling, instructions for use, the production processes and methods at every stage in the life cycle of the supply or service, as well as the evaluation and conformity procedures;

  • Clinical nurse specialist means a registered nurse with relevant post-basic qualifications and 12 months’ experience working in the clinical area of his/her specified post-basic qualification, or a minimum of four years’ post-basic registration experience, including three years’ experience in the relevant specialist field and who satisfies the local criteria.

  • Phase 4 Clinical Trial means a Clinical Trial of a Product conducted after Regulatory Approval of such Product has been obtained from an appropriate Regulatory Authority, which trial is (a) conducted voluntarily by a Party to enhance marketing or scientific knowledge of the Product, or (b) conducted due to a request or requirement of a Regulatory Authority.

  • Development Schedule shall have the meaning set forth in Section 1.1.

  • Commercial solid waste means all types of solid waste generated by stores, offices, restaurants, warehouses, and other nonmanufacturing activities, excluding residential and industrial wastes.