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Subpart A—General

This subpart explains the purpose and scope, definitions, petitions for issuance, amendment, and repel of a standard in 29 CFR 1910. The purpose of these standards is to make the workplace safer and healthier. It explains the applicability of the OSHA standards relevant to the workplaces covered, the geographic location covered, and specific entities (i.e.. Federal agencies) not covered. It also lists regulations that have been incorporated in this standard by reference into 29 CFR 1910 as well as the requirements for nationally recognized testing laboratories. [Pg.457]

7 Definition and requirements for a nationally recognized testing laboratory [Pg.458]

Subpart A General Provisions Subpart B Organization and Personnel Subpart C Buildings and Facilities Subpart D Equipment... [Pg.637]

Subpart A—General Provisions Subpart B—Informed Consent of Human Subjects Subpart C—Protection Pertaining to Clinical Investigations Involving Prisoners as Subjects... [Pg.189]

Subpart A, General Provisions and Definitions. It sets forth the minimum current good compounding practices for the preparation of drug products by state-licensed pharmacies for dispensing and/or administration to humans or animals and includes definitions and requirements, as follows ... [Pg.20]

Part 160 - GOOD LABORATORY PRACTICE STANDARDS Subpart A - General Provisions... [Pg.60]

Part 56—Institutional Review Boards Subpart A—General Provisions... [Pg.74]

Disqualification of an IRB or an institution Part 312—Investigational New Drug Application Subpart A—General Provisions... [Pg.74]

The US FDA GLP regulations (21 CFR 58) are comprised of 11 subparts (A-K), beginning with a definition of the scope and terminology (subpart A, General Provisions), followed by minimal requirements for the following ... [Pg.834]

EPA. 1985b. Determination of reportable quantities. Determination of reportable quantities for hazardous substances. U.S. Environmental Protection Agency. Subpart A - General Provisions. Code of Federal Regulations. 40 CFR 117.3. [Pg.372]

CFR Part 211 Current Good Manufacturing Practice for Finished Pharmaceuticals Subpart A General Provisions 211.1 Scope... [Pg.214]

Subpart A - General provisions Subpart B - Organisation and personnel Subpart C - Buildings and facilities Subpart D - Equipment... [Pg.12]

In addition. Part 385, Subpart A (General) and Subpart E (Hazardous Materials Safety Permits) apply to motor carriers and motor vehicles that transport hazardous materials in intrastate commerce and are subject to 385.403. [Pg.411]

Subpart A — General, outlines the scope of Part 391, and provides a few general exemptions to the driver qualification requirements. [Pg.333]

See other pages where Subpart A—General is mentioned: [Pg.70]    [Pg.214]    [Pg.233]    [Pg.10]    [Pg.487]    [Pg.378]    [Pg.396]    [Pg.189]    [Pg.189]    [Pg.281]    [Pg.126]    [Pg.126]    [Pg.127]    [Pg.59]    [Pg.36]    [Pg.121]    [Pg.43]    [Pg.43]    [Pg.43]    [Pg.141]    [Pg.73]    [Pg.336]    [Pg.1942]    [Pg.26]    [Pg.149]    [Pg.149]    [Pg.705]    [Pg.706]    [Pg.91]    [Pg.127]    [Pg.195]    [Pg.255]    [Pg.283]    [Pg.332]    [Pg.395]    [Pg.403]    [Pg.405]   


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Subpart

Subpart A — General Provisions

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