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FDA Budget Could Hike User Fees, Overseas Inspections

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Budget-conscious firms that do business in China and elsewhere outside the United States may not like what they find in the Food and Drug Administration’s (FDA) request in the 

FDA Offers Salty Recipe for Increased Food Regulation

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It’s actually bigger than a battle over a popular condiment, according to some folks who oppose what they say is the Food and Drug Administration (FDA) overplaying its regulatory hand.

Quality Pro Salaries Keep Pace with Inflation

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(ASQ: Milwaukee, WI) -- The results of ASQ’s 25th annual Salary Survey show strong average salaries for quality professionals in 2011 and fewer lay-offs as companies continue to see the value of quality and its positive impact on an organization.

FDA Reorganization Signals More Inspections for Drug, Device Firms

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Under pressure from all sides, the beleaguered Food and Drug Administration (FDA) keeps announcing new reorganization initiatives, name changes, and all sorts of stuff that would be funny if it was scripted by the same team handling Steve Carell’s departure from

Foreign Exporters Study U.S. Food Safety Law

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The Food and Drug Administration’s (FDA) international program has logged nearly 75,000 hits to its web pages on the new food safety law, as foreign companies that export food to the United States scramble to learn how the law affects them.

Quality by Design Pilot Presents Industry with New Challenges

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What products will be affected by the Food and Drug Administration’s (FDA) quality by design (QbD) stipulation, as outlined in its report, “Pharmaceutical Quality for the 21st Century: A Risk-Based Approach”?

FDA to Set Production Standards for Safer Fruit and Vegetables

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As headlines from Europe implicate tainted vegetable sprouts in more than 4,000 illnesses and dozens of deaths, American consumers may wonder, “Could that happen here?”

Independent Study Finds FDA 510(k) Review Process Has Slowed

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Well, this is getting interesting. For the past several months, we’ve had relatively partisan folks on each side of the medical device industry vs.

FDA Demands Corporate Commitment at PolyCarbon Industries

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Just when you think that the Food and Drug Administration (FDA) has to stick to the script by quoting chapter and verse of current Good Manufacturing Practices (CGMPs), it gets very progressive and offers straight talk about corporate commitment and leadership.

ACLASS’s Greenaway Speaks on Food Safety Modernization Act

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Keith Greenaway, vice president of ACLASS, a brand of ANSI-ASQ National Accreditation Board that provides accreditation, gave a brief talk titled “Focus on Inspections and Compliance” at the FDA Food Safety Modernization Act public meeting held on June 6, 2011.

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