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News
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FDA’s Crowley addresses Unique Device Identification

The U.S. Food and Drug Administration has provided a detailed description of proposed effective dates for Unique Device Identification (UDI) requirements on its Web site.
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Too much medication?
News
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Report says 40% of parents give young kids cough/cold medicine that they shouldn’t

Many parents disregard label warnings. …Meanwhile, FDA’s BeSafeRx provides interactive map tool to protect against fake pharmaceuticals.
Connected world
Column/Opinion
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Attacking 'counterfeit' medications with a broader strategy

New Institute of Medicine report points to a new way of talking about and addressing problematic meds globally, with packaging smack dab in the middle of the issue.
Anaheim Convention Center
News
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Nanotechnology: Observing the regulatory frontier

Nanotechnology, combination products, and regulatory strategies frame the future in medical compliance issues, as noted in Feb. 12 MD&M West conference track.
Avastin ac
Column/Opinion
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Could ‘Big Data’ help thwart counterfeit meds?

Despite numerous anti-counterfeiting products and approaches, the vexing problem continues worldwide.
Almac line
News
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Almac launches U.S. commercial packaging operations

Successful FDA inspection and new client partnership highlight $10 million-plus facility’s opening.
Column/Opinion
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Food safety regulation shoes keep dropping

In the world of food safety, the other shoe dropped in January.
NutraBio bottles
Feature Article
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Nutritional supplement company saves money, reduces waste

NutraBio meets ever-changing labeling demands with digital label printing systems that reduce the need for label inventory and cut costs.
S-ICD
Feature Article
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FDA tracking proposal could require packaging line changes

Medical device makers would need to use automatic identification and data capture technology for marking implantable and all devices and their packaging.
Sales pitch PW
Column/Opinion
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A revolution in drug label regulation?

A federal appeals court recently said FDA could not legally prohibit a drug company salesman from promoting off-label uses of its drug. Here’s what this could mean to drug manufacturers, and to FDA.

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