Regulatory

Healthcare packaging seminar May 6-7, 2014 to address challenges faced in China, including medical package design, validation, and regulatory issues.
News
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First LifePack Forum slated for Suzhou, China

Healthcare packaging seminar May 6-7, 2014 to address challenges faced in China, including medical package design, validation, and regulatory issues.
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By establishing an Office of Pharmaceutical Quality, FDA hopes to spur pharmaceutical manufacturers to address batch process, packaging, and other problems impacting the supply chain.
Feature Article
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FDA wants pharma to move from compliance to quality

By establishing an Office of Pharmaceutical Quality, FDA hopes to spur pharmaceutical manufacturers to address batch process, packaging, and other problems impacting the supply chain.
This photo shows an authentic alli carton.
News
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GlaxoSmithKline voluntarily recalls alli weight loss product

Company believes some packages of the product were tampered with, leading to recall of all alli products from U.S. and Puerto Rico retailers.
Column/Opinion
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Food label changes invoke nutrition, health, history

There were many reactions to the recent announcement by the U.S. Food and Drug Administration of its proposed changes to food nutrition labeling, announced with great fanfare by FDA and first lady Michelle Obama. My reaction was, it made me think of history.
President Richard M. Johnson of The Parenteral Drug Assn.
Column/Opinion
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A Washington perspective on healthcare packaging

Visits to PDA, USP, RAPS, and CPSC reveal what works "Inside the Beltway."
Dr. Michael Drues is President of Grafton, MA-based Vascular Sciences, an education, training, and consulting company. He can be reached on Linkedin®, by phone at 508.887.9486, and by e-mail at mdrues@vascularsci.com
Column/Opinion
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10 questions for the future of medicine, circa 2024

The global healthcare community’s responses to these 10 questions could have a profound impact on the future of medicine—and its packaging.
HealthPack 2014 in Albuquerque included a number of exhbitor booths.
News
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Are medical device manufacturers overwhelmed with standards?

Medical device standards and regulations generate discussion at HealthPack 2014’s opening day.
Desmond Hunt addressed U.S. Pharmacopeia issues at PDA Europe 2014.
News
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PDA Europe addresses regulatory and standards issues

Regulatory and standards agencies must move forward to take into account complex biologics, single-use manufacturing, improved testing methods, etc.
Eric Greenberg is Principal Attorney at Eric F. Greenberg P.C., a law firm that concentrates its practice in food and drug law, packaging law, and commercial litigation. He can be reached at greenberg@efg-law.com or at 312-977-4647.
Column/Opinion
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Packaging adds safety, other benefits

The recently passed DQSA law is an important part of the picture, but only part of the story of how packaging’s role in safety is increasing.
Dirk Rodgers, who contributed to Healthcare Packaging’s Pharmaceutical Serialization Playbook, is an independent consultant and founder of RxTrace.
Column/Opinion
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The future of healthcare supply chain security

We know more about how healthcare supply chain security will work in 2024 than looking forward in any previous 10-year period.

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