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Calibration in the Pharmaceutical Laboratory
 
 
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Calibration in the Pharmaceutical Laboratory (Hardcover)

by Tony Kowalski (Editor) "As the regulation of test and measuring equipment used in pharmaceutical manufacturing and quality assurance is ever increasingly becoming an administrative nightmare with continually moving..." (more)
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Product Description

Product Description
Increasingly, pharmaceutical scientists must not only be specialists in their field but also must be familiar with legislation that governs the use of equipment in the industry. The regulation of test and measuring equipment changes continually as new regulations are introduced. Calibration in the Pharmaceutical Laboratory provides general background on laboratory balances and precision scales, insight into mass measurements and associated errors, and detailed information on key quality issues associated with weighing. Managers responsible for QC and QA will find this book an invaluable tool for setting out SOPs for balances and scales used throughout the manufacturing and testing process.

From the Back Cover
Increasingly, pharmaceutical scientists must not only be specialists in their field but must also be familiar with legislation that governs the use of equipment in their industry. The regulation of test and measuring equipment changes continually as new regulations are introduced and new equipment is developed. Calibration in the Pharmaceutical Laboratory provides general background on laboratory balances and precision scales, insight into mass measurements and associated errors, and detailed information on key quality issues associated with weighing. Managers responsible for QC and QA will find this book an invaluable tool when setting out SOPs for balances and scales used throughout the manufacturing and testing process.
Inside This Book (Learn More)
First Sentence
As the regulation of test and measuring equipment used in pharmaceutical manufacturing and quality assurance is ever increasingly becoming an administrative nightmare with continually moving goalposts and where new regulations could be introduced from either government, the Food and Drug Administration (FDA) or the Medicines Inspectorate, external help is often required from publications that specifically detail plans to incorporate equipment into quality systems. Read the first page
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