FDA

Biosimilars image supplied by Allied Market Research
News
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Report examines biosimilars market drivers

Manufacturers see opportunity as blockbuster biologics face patent expiries, with emerging markets representing an easier ‘launching pad’ for biosimilars/follow-on biologics.
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Credo production line.
Column/Opinion
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Three primary cold chain packaging pain points and priorities

Along with preventing temperature excursions, three priority issues are regulatory compliance, reducing costs, and emerging markets.
Eric Greenberg
Column/Opinion
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Trim the fat, cut the GRAS?

Use it or lose it, goes the old saying. But what happens if you do use it? Why, it makes you want to use it again, of course.
FDA revises proposed Nutrition Facts label rule
News
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FDA revises proposed Nutrition Facts label rule

Aim is to include a daily value for added sugars to help consumers make more informed choices. Public comments welcomed for 75 days from July 24, 2015.
This photo shows capsules with a DNA imprinted on them.
Feature Article
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What’s new in personalized medicine?

A new PwC/Personalized Medicine Initiative Green Paper describes patient benefits. Meanwhile, Grand View Research predicts the global genomics market value to top US$22 billion by 2020.
HealthPack 2016 will be held March 15-17 at the Astor Crowne Plaza in New Orleans.
Feature Article
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Medical device packaging takes center stage at HealthPack

HealthPack 2015 focused on exclusive survey and package design. Meanwhile, HealthPack 2016 venue is established.
Specialty pharmacies, says at least one group, represent the fastest-growing segment of the pharmaceutical market.
News
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Promising future for specialty pharmacies

Taking a quick look at the market and the challenges in what at least one group says represents the fastest-growing segment of the pharmaceutical market.
News
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Fast-tracking medical devices through the FDA

Starting April 14, the new program will help manufacturers of devices for life-threatening, or irreversibly debilitating, conditions get approval faster.
News
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Is lack of standardized medical device labeling harming patients?

The FDA is studying if they should require standardized medical device labeling.
News
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Near record lows for medical device recalls

It's been two years since the FDA saw recall numbers this low.

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