User"s guide to the Contract Laboratory Program.
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User"s guide to the Contract Laboratory Program.

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Published by Office of Emergency and Remedial Response, U.S. Environmental Protection Agency in Washington, DC .
Written in English

Subjects:

  • Hazardous wastes -- United States -- Sampling -- Handbooks, manuals, etc.,
  • Hazardous waste sites -- United States -- Handbooks, manuals, etc.

Book details:

Edition Notes

ContributionsUnited States. Environmental Protection Agency. Office of Emergency and Remedial Response.
The Physical Object
Paginationvii, 69 p. :
Number of Pages69
ID Numbers
Open LibraryOL17661561M

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The CLP User's Guide acts as a reference for theRegions and laboratory contractors to promote consistency in procedures throughout the Regions andensure the proper adherence to CLP requirements. This document along with the CLP Sampler's Guideprovides a thorough overview of . Superfund Analytical Services and Contract Laboratory Program. The Superfund Contract Laboratory Program (CLP) provides analytical services to EPA, the Army Corp of Engineers as well as state, local and Tribal agencies to support Superfund, Brownfields, and other EPA programs. Sampler's guide to the Contract Laboratory Program. Washington, D.C.: Office of Emergency and Remedial Response, U.S. Environmental Protection Agency, [] (OCoLC) Contract Laboratory Program Guidance for Field Samplers This document contains general information about environmental sample collection for the EPA's CLP including minimum CLP requirements, an explanation of the sampling process sequence of events, and information and checklists to help in planning and documenting sampling activities.

  Introduction to the Contract Laboratory Program This document is designed to educate the EPA's Superfund staff and managers on how to obtain laboratory analytical services through the CLP for Superfund, Brownfields, and other sites. CLP users also are encouraged to review the Introduction to the Contract Laboratory Program document that contains a general overview of the CLP, how it works, and how to access the program. The CLP requires samplers to use the functionality provided by the Field Operations Records Management System (FORMS) II Lite™ software, which is the preferred means of creating CLP sample documentation. accreditation to the Illinois Environmental Laboratory Accreditation Program within days of the execution of the contract for which this Statement of Work applies. Failure to apply for and obtain accredi tation from the Illinois Environmental Laboratory Accreditation Program Agency will be grounds for termination of the Size: 1MB. users, and one for contracts. A user address is a hash of a public key; whoever knows the corresponding private key can spend the money associated to that address. Users can create as many accounts as they want, and the accounts need not be linked to their real identity. A contract is an instance of a computer program that runs on the Size: KB.

Page 6 of 43 Laboratory Services Information Manual TEST ORDER ENTRY OUTPATIENTS Laboratory Request Form (Requisition Form) - Physician clients of RCHSD Laboratory are provided with Laboratory Request Forms that contain the physician or practice name and address. The CIPS Contract Management guide is intended to cover all those activities associated with contract management. The activities themselves are divided into two distinct but interdependent phases, upstream and downstream of the award of the contract. The principles in this guide could be applied to.   What the Contract Laboratory Program Does The Contract Laboratory Program’s (CLP) primary service is the provision of analytical data of known and documented quality to CLP customers. The CLP provides data through its chemical analytical services, and has implemented supporting services to ensure that data of known and documented quality is provided to CLP users. Even if the contract laboratory has been inspected by a regulatory agency, the contract giver still has the responsibility to ensure that testing is conducted according to GMP principles and guidelines, marketing authorization and technical agreements.