Xem 1-20 trên 34 kết quả Approval procedures
  • The engineering department staff is responsible for approving, publishing, and distributing the engineering procedure manuals and any subsequent revisions. The manual will be reviewed and updated annually or as required to maintain an effective engineering program. The manual is maintained on a controlled copy basis, with manual holders receiving copies of new or revised pages as they are issued and notices to remove deleted pages. Generally, only manuals that have identification numbers will be controlled and maintained.......

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  • This book covers the method where engineering procedure writers write their own policies, departmental instructions and engineering procedures and obtain approval from the Document Review Board (Ch. 5) and releases them into engineering document control. Engineering document control publishes the manuals and distributes them to end-users.

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  • This document defines: a. the minimum requirements to be used for the development and manufacture of 406 MHz ship security alert system (SSAS) beacons, provided at section 2; and b. the policies, procedures and type approval test methods for obtaining Cospas- Sarsat type approval of 406 MHz SSAS beacons, provided at section 3

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  • All these changes have a huge impact on the way the database query optimizer works. Having user-defined functions deep in- side the query plans makes cost estimation problematic. Having real data with high skew has always been problematic, but in this new world the relational operators are just the outer loop of a non- procedural program that should be executed with the least cost and in parallel. Cost-based static-plan optimizers continue...

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  • These guidelines address methods for: (1) handling of samples as intact soil cores; (2) preserving samples; (3) storing samples in hermetically sealed containers; and (4) minimizing analyte losses due to direct volatilization (both in the field and the laboratory) and biodegradation. Region 9 believes that following these guidelines is an important part of ensuring that accurate concentrations of VOCs are measured.

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  • Many of the world’s problems—violence, overpopulation, substance abuse, poverty, terrorism, infant mortality, HIV/AIDS, chronic disease— involve human behavior. Since countries are increasingly interdependent, cross-national collaboration is imperative. U.S. psychological scientists can take an active role, working with colleagues in and from other countries, to improve the world’s capacity to address these pressing issues. International research collaboration in the psychological, behavioral, and social sciences is critical to improving the quality of peoples’ lives worldwide.

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  • Chapter 18a: Question about COMMUNICATIONS MANAGEMENT 1. Which of the following media can a communicator use to present information? a. b. c. d. Visual Audio and visual Tactile Visual, audio, and tactile 2. The three principal interests in maintaining good document control are: a. Timely communication, collection of performance appraisal data, and assuring proper disposal of sensitive documents. b. Timely communication, maintaining proper approvals, and communication cost control. c. Effective communication, ability to reconstruct why decisions were made, and historical value. d.

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  • International code or standard was developed under procedures accredited as meeting the criteria for American National Standards and it is a U.S. national standard. Standards Committee that approved the code or standard was balanced to ensure that individuals are competent and concerned interests have had a chance to participate. The proposed code or standard was made ​​available for public review and comment that provides an opportunity for additional public input from industry, academia, management agencies, and public at large....

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  • From the early 1970s to mid-1990s, positron emission tomography (PET) as a diagnostic imaging modality had been for the most part used in experimental research. Clinical PET started only a decade ago. 82Rb-RbCl and 18F-Fluorodeoxyglucose were approved by the U.S. Food and Drug administration in 1989 and 1994, respectively, for clinical PET imaging. Reimbursement by Medicare was approved in 1995 for 82Rb-PET myocardial perfusion imaging and for 18F-FDG PET for various oncologic indications in 1999. Currently several more PET procedures are covered for reimbursement....

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  • Once the committee has given a positive opinion on the FP, EuropeAID is responsible for the financing decision procedure. As a general rule, the Commis- sion adopts financing decisions by written proce- dure, or in exceptional circumstances by habilitation procedure. After approval of the FP by the Commission, EuropeAID prepares the Financing Agreement and takes responsibility for ensuring complete consistency between the Financing Proposal and the FA. The FA is based upon a model Financing Agreement, prepared by EuropeAID.

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  • The policy has the simplest format compared to procedures. The cover page could have a header and a footer to capture useful information and approval signatures and subsequent pages will just have a header to link the pages together. The same format is used for all policies, because having them all the same, as much as possible, is more economical. Any time there are variations in thinking patterns, time and money are wasted.

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  • This report has been reviewed in draft form by individuals chosen for their diverse perspectives and technical expertise, in accordance with procedures approved by the NRC’s Report Review Committee. The purpose of this independent review is to provide candid and critical comments that will assist the institution in making its published report as sound as possible and to ensure that the report meets institutional standards for objectivity, evidence, and responsiveness to the study charge.

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  • The Act also allows States to apply to the Secretary to implement a program for regulating organic products produced and handled within that State. The State must have noncompliance, mediation, and appeal procedures that meet NOP regulations to become a State Organic Program (SOP). If approved, the SOP is responsible for the enforcement of NOP regulations within the State. SOPs may also contain more restrictive requirements because of environmental conditions or the necessity for specific production or handling practices particular to that State.

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  • Form DQA (Design Quality Audit Checklist) is used to perform, record, and certify the audit. A non-conformance with the quality process results in the documents being returned to the Originator to bring the package into compliance. If the audit finds all documents in conformance, the DQAM completes and signs Form DQA to document and certify that the QMP requirements have been followed. At the appropriate time, the DQAM also uses Form DQA to certify that the design package is approved for RFC (Refer to section 4.7 RFC Procedure).

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  • An organization needs internal controls to provide greater assurance that they will achieve their operating, financial reporting, and compliance objectives; in other words to help the organization succeed in its mission. Internal control helps ensure that the directions, policies, procedures, and practices designed and approved by management and the board are put in place and are functioning as desired.

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  • What is most needed is to adjust the requirements of SEA and EIA directives. The logical order of these assessments should be ensured, as should the respect of the results of SEA in subsequent EIA procedures. Repeated assessment (on the same level of details) shall be avoided, whereas at the same time the availability of information from earlier relevant SEA procedures should be ensured in subsequent EIA procedures.

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  • For subsequent analysis of the specimen, the needles may be rinsed into a physiologic solution, tissue culture medium, transportation medium or proprietary fixative for liquid based processing. Needles should not be re-sheathed using a two handed technique and instead should be discarded directly into an OSHA approved sharps disposal container. 9 For cystic lesions, remove as much fluid as possible. The cyst fluid can be handled as a liquid specimen. If there is a residual mass, the procedure for solid lesions as described above should be followed.

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  • On the federal level, three agencies regulate ART. The Centers for Disease Control and Prevention (CDC) collects and publishes data on ART procedures. The Food and Drug Administration (FDA) controls approval and use of drugs, biological products, and medical devices and has jurisdiction over screening and testing of reproductive tissues, such as donor eggs and sperm. The Centers for Medicare and Medicaid Services (CMS) is responsible for implementation of the Clinical Laboratory Improvement Act to ensure the quality of laboratory testing....

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  • This report has been reviewed in draft form by persons chosen for their diverse perspectives and technical expertise in accordance with procedures approved by the National Research Council’s Report Review Committee. The purposes of this review are to provide candid and critical comments that will assist the institution in making the published report as sound as possible and to ensure that the report meets institutional standards of objectivity, evidence, and responsiveness to the study charge.

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  • Other than the mandatory audits of publicly financed Presidential campaigns and national party convention committees, Section 438(b) of the Federal Election Campaign Act (FECA) allows the Commission to audit a committee if its reports do not meet the threshold require- ments for substantial compliance with the Act. Campaign Finance Analysts in the Commis- sion’s Reports Analysis Division (“RAD”) review every report following detailed procedures approved by the Commission.

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