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Search Results "Regulatory Process"
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- DOE "Dear Colleague" Letter: Charter Schools, (May 14, 2014)
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2. Treatment of WCAG 2.0
However, rather than using the text of relevant portions of WCAG 2.0 verbatim, the Board restated those Success Criteria in mandatory language thought to be better suited for a regulatory...
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Relationship to Other Laws
The Department recognizes that DOT has its own independent regulatory responsibilities under subtitle B of title II of the ADA....
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Injunctive Relief
Paragraph 15; Dates and attendance logs of HIV Training(s); A catalog containing the name(s) of any detainees who self-identify as having HIV during UPDC’s intake process...
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28 CFR Parts 35 and 36, Nondiscrimination on the Basis of Disability; Accessibility of Web Information and Services of State and Local Government Entities and Public Accommodations (ANPRM)
proposed rulemaking (ANPRM) in order to solicit public comment on various issues relating to the potential application of such requirements and to obtain background information for the regulatory...
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Section 36.302(f) Ticketing (Section-by-Section Analysis)
Through the investigation of complaints, its enforcement actions, and public comments related to ticketing, the Department is aware of the need to provide regulatory guidance to entities...
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Sections 35.108(d)(1)(ii) and 36.105(d)(1)(ii)—Primary Object of ADA Cases
The Department retained the language of these rules of construction in the final rule except that in the title III regulatory text it has changed the reference from ‘‘covered entity’’ to...
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28 CFR Parts 35 and 36 Amendment of ADA Title II and Title III Regulations To Implement ADA Amendments Act of 2008 - Final Rule
case the citation is to section 2 of Public Law 110–325, September 25, 2008.1 This final rule was submitted to the Office of Management and Budget’s (OMB) Office of Information and Regulatory...
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Medical Device Manufacturers
These economic impacts are not regulatory costs and are not generally social costs because for the most part, one manufacturer’s loss is another manufacturer’s gain....
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Appendix E to Part 37—Reasonable Modification Requests
Importantly, reasonable modification applies to an entities' own policies and practices, and not regulatory requirements contained in 49 CFR parts 27, 37, 38, and 39, such as complementary...
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II-3.7200 Licensing
A public entity may not discriminate on the basis of disability in its licensing, certification, and regulatory activities....
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2. Accommodation in testing
(Sensory skills include the abilities to hear, see and to process information.)...
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11B-104.1.1 Construction and manufacturing tolerances
Conventional industry tolerances recognized by this provision include those for field conditions and those that may be a necessary consequence of a particular manufacturing process....
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E. Community Evacuation and Transportation
One step that can significantly increase the effectiveness of your planning process is to create a voluntary, confidential registry of persons with disabilities who may need individualized...
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Statutory Background
Through this process, the Board and the standard-setting agencies coordinated extensively to minimize any differences between the Board’s guidelines and their eventual updated standards....
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8. Providing Qualified Readers
When an applicant or employee has a visual disability, the employer and the individual should use the "process" outlined in 3.8 above to identify specific limitations of the individual in...
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The invisibility of people with disabilities
If more detail is needed, samples of more in-depth questions that can be used or integrated into the registration process including drop-down options in an electronic health record are provided...
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Voluntary Action Plan for Accessible Websites
Voluntary Action Plan for Accessible Websites Establish a policy that your web pages will be accessible and create a process for implementation....