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Quality control management

The quality control manager is responsible for following the procedure. The quality assurance manager is responsible for SOP compliance. [Pg.191]

Check Lists. Tables I and II list groups of quality control check points which should be monitored for each wine lot during the corresponding phases in the winery. The quality control manager should... [Pg.224]

The responsibilities for suitable validated analytical methods, however, do not rest solely in the analytical method development group. Today the analytical function uses new and sophisticated chromatographic and other instrumental techniques that require a high level of technical expertise. It is the responsibility of quality control management to ensure that its staff is adequately trained and its laboratories properly equipped so that new analytical methods can be properly transferred from an analytical methods group to the quality control department. A mutual understanding of each other s responsibilities and limitations is... [Pg.204]

Personal communication, Hein Schroder, Quality Control Manager, South Africa Cotton Board, 1995. [Pg.167]

Figure 19-1 The cost of quality in terms of the costs of conformance and the costs of nonconformance to customer requirements. (From Westgard jO, Barry PL, Cost-e/fect/ve quality control Managing the quality and productivity of analytical processes. Washington DOAACC Press, 1986.)... Figure 19-1 The cost of quality in terms of the costs of conformance and the costs of nonconformance to customer requirements. (From Westgard jO, Barry PL, Cost-e/fect/ve quality control Managing the quality and productivity of analytical processes. Washington DOAACC Press, 1986.)...
Westgai d, J. O., Barry, P. L. (1986). Cost-effective Quality Control Managing the Quality and Productivity of Analytical Processes. Washington, DC AACC Press. [Pg.14]

The revised draft requirements for GMP are presented in three parts. Part One, "Quality management in the drug industry philosophy and essential elements", outlines the general concepts of quality assurance as well as the principal components or subsystems of GMP, which are joint responsibilities of the top management and of production and quality control management. These include hygiene, validation, self-inspection, personnel, premises, equipment, materials, and documentation. [Pg.18]

Starting and packaging materials Before releasing a starting or packaging material for use, the quality control manager should ensure that the materials have been tested for conformity with specifications for identity, strength, purity, and other quality parameters. [Pg.35]

A self-inspection team shall be organized by the drug manufacturing enterprise and the production and quality control management shall be periodically inspected. The enterprise in which the self-inspection has been carried out shall receive the supervision of health authorities. [Pg.355]

Manufacturing Control Manager and Quality Control Manager.. [Pg.451]

The manufacturing control manager shall not hold the position of a quality control manager concurrently. [Pg.453]

To supervise the manufacturing control manager and the quality control manager. [Pg.453]

The manufacturer shall have the quality control manager perform systematically and appropriately the following duties related to the quality control in accordance with the product master formula or the quality control standard code ... [Pg.455]


See other pages where Quality control management is mentioned: [Pg.632]    [Pg.93]    [Pg.102]    [Pg.801]    [Pg.802]    [Pg.803]    [Pg.105]    [Pg.120]    [Pg.221]    [Pg.632]    [Pg.385]    [Pg.180]    [Pg.634]    [Pg.317]    [Pg.450]    [Pg.56]    [Pg.185]    [Pg.1516]    [Pg.354]    [Pg.451]    [Pg.452]    [Pg.453]    [Pg.455]    [Pg.456]    [Pg.469]   
See also in sourсe #XX -- [ Pg.199 , Pg.200 ]

See also in sourсe #XX -- [ Pg.199 , Pg.200 ]




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