thus concludes that the potential benefits of the MDE Standards justify its potential costs; that the MDE Standards will impose the least burden on society, consistent with achieving the regulatory...
Search Results "Regulatory Analysis"
Commonly Searched Documents
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C. Costs and Benefits
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F. The Department's Rulemaking History Regarding Captioning and Video Description
The NPRM asked exploratory questions about, but proposed no regulatory text for, movie captioning and video descriptions....
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III 3.11000 Insurance
Under some State regulatory schemes, however, insurers may have to file such actuarial information with the State regulatory agency, and this information may be obtainable at the State level...
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Introduction
As further discussed under the Statutory and Regulatory Background, these laws require other federal agencies to issue regulations which include accessibility standards for the design, construction...
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1. New Format for Guidelines
We removed the List of Figures and Index in Appendix E because it did not contain regulatory material....
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Structural Impracticability—28 CFR 35.151
As emphasized above, HUD cannot allow the use of an alternative standard which conflicts with HUD’s regulatory requirements and may reduce accessibility in housing settings without the opportunity...
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State and local vocational rehabilitation agencies
The President's Committee on Employment of People with Disabilities provides technical information, including publications with practical guidance on job analysis and accommodations....
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Certification.
The specific changes to subpart F are described below in the section-by-section analysis....
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Section 37.139 Plan Contents
The Department's regulatory impact analysis discussing the probable costs involved in implementing this rule places the possible percentage of population who would be eligible for paratransit...
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Emphasis on Limitations Instead of Outcomes
The Committee believes that the comparison of individuals with specific learning disabilities to ‘‘most people’’ is not problematic unto itself, but requires a careful analysis of the method...
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3. Relationship between Functional Performance Criteria and Technical Provisions
The Board discusses this issue in further detail below in Section V.C (Major Issues - Functional Performance Criteria), Section VI.B (Section-by-Section Analysis - 508 Standards: Application...
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1.0 Background
In this report, we present a comparative analysis of research and standards on wheeled mobility in the U.S., the U.K., Australia and Canada....
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Notes
Analysis of Seat Height for Wheeled Mobility Devices. 2011. 3. The Impact of Transfer Setup on the Performance of Independent Transfers: Final Report....
- Amendment of Americans With Disabilities Act Title II and Title III Regulations To Implement ADA Amendments Act of 2008
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Safe harbor and other proposed limitations on barrier removal.
The specific proposals are addressed in the discussion of barrier removal in the section-by-section analysis of § 36.304 below. The Department is not proposing to adopt Option III. ...
- NewVision™ Curb Ramp Inventory System (NVCRIS)
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11B-224.7.2 Multi-bedroom housing units with adaptable features
mobility features at housing at a place of education are required to comply with the standards for transient lodging in the ADAS by the United States Department of Justice (USDOJ) in its regulatory...
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R218 Doors, Doorways, and Gates
The AASHTO Guide recommends alternative methods to control unauthorized motor vehicle entry to shared use paths, including posting regulatory signs prohibiting motor vehicle entry and targeted...
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BACKGROUND
Access Board to promulgate regulatory standards “setting forth the minimum technical criteria for medical diagnostic equipment used in (or in conjunction with) physician's offices, clinics...
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F. Chapter 5: Doorways, Circulation Paths, and Fare Collection Devices
Other provisions in this chapter have also undergone modest editorial changes aimed at clarifying or simplifying the regulatory text....
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III. Statutory Background
The Access Board is taking this approach because we feel that the two sets of requirements, by virtue of their subject matter, are inextricably linked from a regulatory and policy perspective...
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Introduction
This version includes regulatory updates along with practical guidance from a host of meeting planning professionals, subject matter experts, and even June Kailes herself....
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Other relevant federal rules and guidance documents
The FDA-CDRH may develop a guidance document to inform manufacturers how it intends to apply its regulatory authority to clearance or approval of medical devices addressed in the Access...