Regulator parts

Air Contaminants—Permissible Exposure Limit," Title 29 Code of Federal Regulations Part CFR 1910.1000, OSHA, 1989, p. 3112. 

Title 21, Code of Federal Regulations, Parts 210 and 211, Government Printing Office, Washington, D.C. 

Portable tanks, drums, or bottles are shipped by rail, ship, air, or truck. Portable tanks containing hazardous materials must conform to DOT regulations. Parts 173 and 178, Siibpart H. 

OSHA. 1989, Air Contaminants Permi.ssible Exposure Limits. Title 29 Code of Federal Regulations, Part 1910.1000. U.S. Department of Labor. OSHA 3112. 

Detailed regulations supporting the Acts are published principally in Title 21 of the Code of Federal Regulations (21 CFR). An outline of the main sections of the Title is shown in Table 1.6. Regulations in support of veterinary biologies are contained in Title 9 of the Code of Federal Regulations, Parts 101-123 (see Table 1.7). 

Table 5.4 Code of Federal Regulations Parts relevant to Clinical Trials.

Figure 11.4 Core CMP regulations as set out in Chapter 21 of the US Code of Federal Regulations, Part 211 (21 CFR 211).

This pigment is recognized by the U.S. Food and Drug Administration (21 Code of Federal Regulations, Part 73) as a color additive exempted from certification (Subpart A, Foods, Section 73.35, Astaxanthin). Formulations containing astaxanthin include soft gelatin capsules containing 100 mg equivalents of total carotenoids, a skin care... 

NRC = Nuclear Regulatory Commission, Title 10, Code of Federal Regulations, Part 20... 

NOP (National Organic Program)/USDA (2000) 7 Code of Federal Regulations Part 205. 

Volume 139. Cellular Regulators (Part A Calcium- and Calmodulin-Binding Proteins)... 

Volume 255. Small GTPases and Their Regulators (Part A Ras Family)... 

Volume 256. Small GTPases and Their Regulators (Part B Rho Family) Edited by W. E. Balch, Channing J. Der, and Alan Hall... 

Anon. Code of Federal Regulations Part 448.25 April 1, 1978. 

Specific requirements on content and format of labeling for human prescription drugs warnings Title 21 Code of Federal Regulations, Part 201.57(e), pp. 23, revised 2003. 

New York DEC. Supporting Documents for Chemical Bulk Storage Regulations, Parts 595, 596, and 597 NYS Department of Environmental Conservation Albany, NY, October 1987. 

The action levels are established and revised according to criteria specified in Title 21, Code of Federal Regulations, Parts 109 and 509 and are revoked when a regulation establishing a tolerance for the same substance and use becomes effective. 

Eood and Drug Administration (EDA). Investigational New Drug Application. 21 Code of Federal Regulations Part 312. Washington DC National Archives and Records Administration, 1998. 

Eood and Drug Administration (EDA). Einandal disclosure by cUnical investigators. Title 21 Code of Eederal Regulations Parts 54,312,314,320,330, 601, 807. Federal Register 1998 63 5233-54. 

The incorporation of 3H from [3H]arabinose into Fer-Ara2 units showed a lag of about 4.2 min, after which it too became linear. This means that as little as 0.7 min after their incorporation into a (possibly still nascent) polysaccharide, [3H]arabinose residues were susceptible to feruloy-lation. The feruloylation reaction is thus likely to have been occurring in the endomembrane system, co-synthetically, as one of the highly regulated parts of the sophisticated polysaccharide-biosynthetic machinery. This can be compared to the co-translational modification known to occur in many proteins. 

Good Laboratory Practice Regulations, Part 58 (21CFR), Food and Drug Administration, Washington, D.C. 

Chapter 3 examines the new FDA regulation, Part 11, and its impact on a GLP laboratory setting. This chapter argues that Part 11 is a de facto extension of the GLPs and represents a historical update of the GLP regulation. 

Federal law relating to biological products Code of Federal Regulations, parts 600 to 680. 

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