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Clearing the Air on Residual Solvents
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| By
Maribel Rios
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USP 467 Residual Solvents will take effect on July 1, 2008. But does the industry understand these specifications—and is it prepared?
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Quality Systems for Drugs and Biologics
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| By
Andrew G. Edwards
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FDA is modernizing and streamlining current good manufacturing practices. The author examines FDA's evolving approach to quality systems and how a manufacturer can implement a quality system framework.
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Charting Dosage-Form Manufacturing
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Patricia Van Arnum
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Contract manufacturers expand capabilities in aseptic processing, clinical-trial materials supply, and cytotoxic manufacturing.
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AIM-less
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Control, a senior compliance officer
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If at first the product fails, then inspect, inspect again
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Patents "R" Us
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Michelle Hoffman
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Can an overload of patent applications lead to the US' demise as a scientific leader?
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You're Telling Us...
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| By
Alexis Pellek
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PharmTech's polls feature user feedback on issues facing the pharmaceutical industry.
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Coming Down the Pike: Sirtuins
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| By
Michelle Hoffman
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Text sirtuins are the new kinases, according to a presentation given last month at the JP Healthcare Investors Conference in San Francisco by Sirtis CEO Christoph Westphal.
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In the Field
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A news roundup for February 2008.
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Report from: Europe
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Sean Milmo
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A wave of pharmaceutical expansions is expected in Europe this year, surprisingly by Indian companies.
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In the Spotlight
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Jacketed hose provides cleanability; Stopper prevents product waste; Accessories control temperature precisely
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