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Regulatory requirements overview

The handbook additionally provides an extensive overview and comparison of commercially available computer systems and software for chemical emergency planning. This section provides technical guidance for hazard analysis and identification implementing regulatory requirements and descriptions of computer applications and systems applicable under SARA Title III. [Pg.320]

This paper provides an overview of SOPs including regulatory requirements, and guidelines for establishing and maintaining a system of SOPs. [Pg.47]

In this section, an overview of the results should show that the regulatory requirements for approval have been met by adequate and well-controlled studies that support the claimed effect. This is especially important if results are inconsistent or marginal. An examination of study-to-study differences in results, effects in subsets of the treated population, dose-response information, and comparisons with alternative drugs should be addressed. A description of the information to be included in this section is contained in the outline provided earlier in this chapter. [Pg.136]

Overview of Regulatory Environment/Background Regulatory Authorities Regulatory Requirements and Procedures Application for a Marketing Authorization (MA)... [Pg.12]

An overview of the results should show that the regulatory requirements for approval have been met by adequate and well-controlled trials that support the claimed effect. This... [Pg.129]

This brief overview cannot identify all regulatory requirements which may apply to a site s waste. However, it is the responsibility of the site to do so. [Pg.40]

We will give an overview of the current digital I C QA requirements to show their complexity and overwhelming document size. Then we will ejq)lain relevant regulatory requirements needed when applying RIPBR to digital I C QA programs. [Pg.70]

This short summary demonstrates that each company has selected a niche application to focus on for their success. The wound dressings have been in the market for some time, while the thermogel applications are apparently still in the regulatory approval process. This is more an indication of the divide in meeting regulatory requirements between external medical products and internal implants rather than product shortcomings. Clearly, this overview indicates that chitin and chitosan-based medical products can be termed commercially successful and this augments well for the future of chitin and chitosan in biomedical research and applications that reach commercialization. [Pg.407]

M. Mady, Global food contact regulatory requirements an overview, PIRA s Global Food Contact Legislation Conference, Alexandria, VA, April 3-4, 2008. [Pg.188]

The focus of this book concerns the properties and the accepted means of transportation, storage, and handling of compressed gases. This handbook is simultaneously intended as an overview of the subject and a source of supplementary information. It is also intended to serve as a guide to pertinent federal regulatory requirements and published standards of the Compressed Gas Association and other standards-developing organizations. [Pg.716]

Overview of partitioning and fate of contaminants retention, retardation and regulatory requirements... [Pg.3]

An overview of the regulatory requirements for animal testing of chemicals contained in these acts is provided in table 5.1. [Pg.58]


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See also in sourсe #XX -- [ Pg.279 ]




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Regulatory requirements

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