MATERIAL INCORPORATED BY REFERENCE

All materials incorporated by reference are available for inspection at the Federal Motor Carrier Safety Administration, Federal Motor Carrier Safety Administration, Office of Enforcement and Compliance (MC-EC), 1200 New Jersey Ave., SE., Washington, DC 20590-0001 and the National Archives and Records Administration (NARA). For information on the availability of this material at NARA, call (202) 741-6030, or go to http Iwww.archives.gov federal register I code of federal regulations I ibr locations.html. 

Waste solids are defined as heterogeneous materials that range from sticky, viscous, or tarry material to dry solid particulates. Special techniques for the treatment of oily, gummy, and adhesive materials (e.g., addition of anhydrous sodium sulfate or silica gel) are specified in the protocol. The gravity phase-separation procedure (24 h at 4 °C) developed by the Environmental Waters and Waste Water Work Group is incorporated by reference to address the removal of liquids from waste solids samples. The waste solids protocol can also be applied to solids partitioned from aqueous or nonaqueous liquids or from gaseous media. 

Liquid means a material that has a vertical flow of over two inches (50mm) within a three-minute period, or a material having one gram or more liquid separation, when determined in accordance with the procedures specified in ASTM D 4359-84, Standard Test Method for Determining Whether a Material is a Liquid or a Solid, 1990 edition, which is incorporated by reference. US 130.5... 

Numerous standards and publications of such organizations as the American National Standards Institute (ANSI) and the American Society for Testing and Materials (ASTM) are referenced throughout the packaging regulations, and are made a part of the regulations by an incorporated by reference provision. A complete listing of these materials is provided in 49 CFR 171.7. 

Who Employees who may be exposed to airborne 4,4 -Methylenedianiline (MDA) at or above its action level or where dermal exposure to MDA can occur. (Note the standard does not apply to finished articles that contain MDA or to materials in any form that contain less than 0.1% MDA by weight or volume.) Also, this standard incorporates by reference 1910.38, 1910.1200, and 1910.134, which have additional training requirements. Also, any person who cleans or launders contaminated protective clothing is to be informed of the hazards of exposure to MDA. In addition, the employer must provide specified information to the physician who is conducting medical surveillance, and the employee is to receive a copy of the physician s written opinion within fifteen days after the employer receives it. 

Note "Gases which cause or contribute to the combustion of other material more than air does means pure gases or gas mixtures with an oxidizing power greater than 23.5% (as determined by a method specified in ISO 10156 or 10156-2 (incorporated by reference. See 1910.6) or an equivalent testing method.)... 

Who Employees occupationally exposed to acrylonitrile (AN). The standard does not apply to processing, use, and handling of finished polymers (and products made from polymers) of ABS resins, SAN resins, nitrile barrier resins, solid nitrile elastomers, acrylic and modacrylic fibers, and solids made from or containing AN that will not be heated above 170 degrees F. (Also exempt are other AN materials that are not capable of releasing specified amounts of airborne I AN.) Also, this standard incorporates by reference 1910.132 and 1910.134,... 

This section should provide a listing of the topical reports that are incorporated by reference as part of the SAR. Results of tests and analyses (e.g. results of manufacturers material tests and qualification data) may be submitted as separate reports. In such cases, the reports should be hsted in this section and referenced or summarized in the appropriate section of the SAR. 

A DMF provides (incorporates) information by reference and permits the holder to authorize other persons to disclose information in support of an application. Usually, a DMF may only be accessed (reviewed) by the FDA if the holder of the drug application provides the FDA with authorization (by incorporation), in writing, with two copies, dated, with the DMF number, name of holder, name of material, specific product, reference number/volume, page number, name of authorized persons, and a statement of commitment that the DMF is current. The letters filed to the DMF must have the original signature, typed name, and title of the authorizing person on... 

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