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Validating Pharmaceutical Systems - Good Computer Practice in Life Science Manufacturing (Hardcover, New)
Loot Price: R5,996
Discovery Miles 59 960
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Validating Pharmaceutical Systems - Good Computer Practice in Life Science Manufacturing (Hardcover, New)
Expected to ship within 12 - 19 working days
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All too often, the words "computer validation" strike terror into
the hearts of those new to the process and may even cause those
familiar with it to tremble. Validating Pharmaceutical Systems:
Good Computer Practice in Life Science Manufacturing delineates
GCP, GLP, and GMP regulatory requirements and provides guidance
from seasoned practitioners on how to fulfill them. John Andrews
and his team tackle the perceived complexities surrounding the
validation of a wide variety of automated systems. Sprinkled with
case studies and real-life examples, the book offers a step-by-step
review of topics such as planning, design, auditing, risk
management, and specification. The in-depth, by example coverage
demystifies the challenges of manufacturing execution systems(MES),
laboratory information management systems(LIMS), and network
qualification. The first section examines the different levels of
automated systems used throughout the drug development,
manufacture, and delivery lifecycle, using the GAMP 4 lifecycle
approach to their validation. The second section uncovers some
real-life applications of GAMP 4 to different areas of the
regulations such as GLP, GCP, GMP, and GDP. The book explores some
of the latest thinking on computer validation and reflects changes
that have occurred in the industry since the early days of
validation. The contributors are a deliberate blend of those who
have faced the problems of the 1990s and the Y2K controversies and
those who have more recently arrived on the scene and made an
impact on the perception of validation of automated systems across
the field of GxP. They do more than show you how to do the right
thing; they show you how to do the right thing in compliance with
regulations.
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