Regulatory

The first PEN bottle of Pulmotil AC to reach the marketplace was the 250-mL size, shown here with its extended text label. The l
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Lilly likes PEN for veterinary product

A new treatment for respiratory problems in pigs and chickens is administered in the field, where the breakability of glass packaging is a concern. A homopolymer PEN bottle provides a shatter-resistant answer and delivers all the shelf life needed.
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Less red tape?

The new Transatlantic Economic Partnership (TEP) announced earlier this year as part of an effort to promote freer international trade could eliminate numerous trade barriers and "miles of red tape," according to GMA.
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FDA proposes labeling for nonpasteurized juices

Agency specifies explicit warning statement for juices that aren't pasteurized. But NFPA wanted more.
Materials Product Brief
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Ampacet Corporation : Concentrates for metallocenes

Ampacet Corp. (Tarrytown, NY) has published a foldout directory that lists 16 of its most popular concentrates for metallocene-based resins. For each product, there are specifications concerning carrier-resin requirements, important product properties and regulatory status.
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Food safety update

President Bill Clinton proposed to create a Joint Institute for Food Safety Research that will develop a strategic plan for conducting food safety research consistent with his Food Safety Initiative.
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Juice warnings, not pasteurization

The Food and Drug Administration issued a final rule on July 8 requiring warning labels on fresh, unpasteurized juices. The requirement applies to all processors that package untreated juice for off-site consumption, including retailers such as grocery stores that squeeze and bottle juice for home use.
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Packaging suppliers in headlights of MACT truck (sidebar)

OSHA complicates EPA compliance
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Codex divided on biotech labeling

The Codex Committee on Food Labeling appears divided over which biotech food labeling recommendations to adopt. It is choosing whether to emulate the U.S.
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Pregnancy labeling changes

FDA plans to revise its regulatory requirements for the pregnancy section of pharmaceutical labeling. An advanced notice of proposed rulemaking will put forth "preliminary proposals for changing the current requirements and will invite comments on all aspects of the notice." This is a long-term action and FDA gave no timetable.
To help the company make the package design conversion, Interbrand Gerstman+Meyers tailored its Brand Wizard software program fo
Feature Article
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Multinational pharmaceutical maker designs standards

Newly merged Hoechst Marion Roussel gets design help to unify the look of primary packages produced anywhere in the world. Package type and size standards are the next step.

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