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Industry News: Page 276
Regulatory
Want to prevent knock-offs? Focus on spelling, bar codes
Counterfeiters have become quite good at copying package components and color. Their weakness often lies in on-pack spelling accuracy and including a bar code.
December 23, 2009
Regulatory
Solid-dose authentication technology
December 21, 2009
Regulatory
FDA warns online offenders
FDA addresses online drug claim offenders in what could be a glimpse into the future of enforcement actions.
December 21, 2009
Medical Device/Packaging
Nanotechnology in packaging presents rewards and risks
Nanotechnology is not without risks, but it packs potential for packaging applications and medical breakthroughs.
December 21, 2009
Adherence/Delivery
Crestor closer to expanded use
FDA advisory committee voted 12 to 4 (one abstaining) to broaden use of cholesterol-lowering Crestor to people with normal cholesterol and no history of heart disease.
December 21, 2009
Regulatory
Counterfeit products gateway to real thing?
A new study suggests counterfeit products can create brand loyalty. Don't you believe it!
December 17, 2009
Regulatory
FDA Expands Presence Outside U.S. with Opening of Mexico City Post
As part of its continuing effort to buttress food and medical product safety in this country by working with its regulatory partners overseas, the U.S. Food and Drug Administration today announced the opening of its Mexico City post.
December 15, 2009
Regulatory
Validation insights for medical device packaging
Medical device packaging validation can be confusing, so here are a few helpful resources to guide your efforts.
December 15, 2009
Regulatory
EU encounters alarming counterfeit numbers
Despite technological advances, counterfeit drugs continue to flourish.
December 11, 2009
Regulatory
Alka-Seltzer Plus Day & Night Cold Formula Liquid Gels - Incorrect Packaging
Bayer Consumer Care and FDA notified Consumers of a recall of a single product lot of the combination package of Alka-Seltzer Plus Day & Night Cold Formula Liquid Gels.
December 9, 2009
Regulatory
Compliance Checklist for FDA-regulated Companies Now Available from Dickson Company
Worldwide food and drug companies selling to the U.S. market can now obtain a free FDA 21 CFR Part 11 Checklist to ensure full regulatory compliance of their environmental monitoring practices.
December 7, 2009
Labeling/Printing
Steris System 1 Processor: FDA Notice and Recommendations
FDA notified healthcare facility administrators and infection control healthcare professionals of important information regarding the regulatory status of the STERIS System 1 Processor (SS1) used in surgical and endoscopy suites for reprocessing, i.e., sterilizing or disinfecting, medical devices.
December 7, 2009
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