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Industry News: Page 271
Regulatory
Sproxil's brand authentication technology earns IBM, MITX honors
Mobile phone technology allows users in third-world countries to determine if a packaged product is genuine or counterfeit.
July 22, 2010
Regulatory
Arava (leflunomide): Boxed Warning - Risk of Severe Liver Injury
AUDIENCE: Rheumatology, Family Practice
July 16, 2010
Regulatory
Uptick forecasted in healthcare M&A activity
Study reports findings based on interviews with more than 75 U.S. healthcare investors covering various life science sectors.
July 16, 2010
Regulatory
DDL, Medical Device Package Testing Firm, Announces their Agreement with CITECH
DDL, announces a cooperative agreement with Pennsylvania-based CITECH, whereby DDL will be taking on testing that was formerly conducted by CITECH.
July 14, 2010
Regulatory
Genzyme, Hospira reach expanded fill and finish manufacturing deal
Follows consent decree with the FDA that said Genzyme had to move fill and finish operations out of its Allston, MA facility.
July 12, 2010
Traceability/Serialization
Mettler-Toledo Hi-Speed to Host Live Webinars in July and August
Pharmaceutical Serialization - Choosing the Right Equipment Supplier for an Effective Strategy.
July 8, 2010
Regulatory
Tamiflu: Counterfeit Product Sold on Internet
Fraudulent product is dangerous to patients allergic to penicillin.
July 7, 2010
Regulatory
Avandia controversy escalates
One Senator and one member of Congress are calling on the FDA to pull from the market the diabetes drug Avandia because of safety concerns. It's the latest flare-up of a firestorm of controversy--and a window into several important issues.
July 2, 2010
Regulatory
May 2010 Drug Safety Labeling Changes
23 Medical Product Labels with changes to Boxed Warning, Warnings, Contraindications, Precautions, Adverse Reactions.
June 28, 2010
Regulatory
Vitamin D Supplement Products: Medication Use Error
Some liquid Vitamin D supplements sold with droppers that could allow harmful amounts of Vitamin D to be dispensed.
June 28, 2010
Regulatory
FDA Takes Action Against California Soy-Product Manufacturer Lifesoy
Products made under conditions that violated federal law.
June 18, 2010
Regulatory
GSK readying for France's CIP13 deadline
With France's CIP 13 coding requirements due to take hold Jan. 1, 2011, GlaxoSmithKline reportedly is becoming 'serialization-ready'.
June 18, 2010
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