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Good Automated Manufacturing Practices GAMP

Note The instruments used in the laboratories vary significantly in the design and operation complexity. The validation requirements should reflect the level of complexity of the instrument. It is obvious that the amount of effort required to validate a simple pH meter will be different from that required for a fully automated dissolution system. The Good Automated Manufacturing Practice (GAMP)... [Pg.141]

The Good Automated Manufacturing Practices (GAMP) Forum has developed guidelines for computer validation [5] and a draft guidance on quality assurance of information technology (IT) infrastructure [6]. [Pg.256]

Good Automated Manufacturing Practices (GAMP), February 1994... [Pg.24]

Trill, A.J. (1995), EU GMP Requirements and the Good Automated Manufacturing Practice (GAMP) Supplier Guide for the Validation of Automated Systems for Pharmaceutical Manufacturing, Pharmaceutical Engineering, May/June, pp. 56-62. [Pg.959]

Good Automated Manufacturing Practice (GAMP) Forum,... [Pg.137]

The good automated manufacturing practice (GAMP) guide for validation of automated systems in pharmaceutical manufacture (GA.MP4) ISPE - International Society for Pharmaceutical Engineering, December 2001. [Pg.458]

See other pages where Good Automated Manufacturing Practices GAMP is mentioned: [Pg.226]    [Pg.407]    [Pg.145]    [Pg.267]    [Pg.283]    [Pg.224]    [Pg.517]    [Pg.145]    [Pg.267]    [Pg.1]    [Pg.78]    [Pg.136]    [Pg.162]    [Pg.262]    [Pg.311]    [Pg.483]   
See also in sourсe #XX -- [ Pg.226 ]



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