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Supplier News

The latest supplier news from Healthcare Packaging
Regulatory
DDL, Medical DevicePackage Testing Firm, Announces their Agreement with CITCH
DDL, a leader in medical device package, product, and material testing, announces a cooperative agreement with Pennsylvania-based CITECH, whereby DDL will be taking on testing that was formerly conducted by CITECH.
September 30, 2010
Home
Label Technology Recognized for Superior Printing Quality
Label Technology, Inc., a printer and converter of flexible packaging and pressure sensitive labels, is proud to announce that they received three industry awards for printing distinction from packagePrinting's 2010 Excellence Awards Competition.
September 16, 2010
Package Development
Keystone Folding Box Company Joins Healthcare Compliance Packaging Council (HCPC)
Alliance Helps Strengthen Company's Leadership Position in Unit-Dose Packaging for Pharma.
September 16, 2010
Regulatory
The August 2010 FDA Patient Safety News is now available...
You can find more information about FDA Patient Safety News, and watch or download the video program on our web site . Stories in the August 2010 edition include:
August 12, 2010
Regulatory
Revivexxx Extra Strength: Recall - Undeclared Drug Ingredient
AUDIENCE: Consumer
August 12, 2010
Regulatory
Solo Slim, Solo Slim Extra Strength: Recall - Undeclared Drug Ingredient
AUDIENCE: Cardiology, Consumer
August 12, 2010
Regulatory
Novacare LLC Products: Recall - Undeclared Drug Ingredient
Products sold under the following names: Stiff Nights, Aziffa, Size Matters, Erex, Mojo, Hard Drive, Eyeful, Red Magic, Straight Up, Zotrex, Monster Excyte, WOW, Xaitrex, Verect, Prolatis, Xytamax, Maxyte, Libidinal, OMG, OMG45, and Zilex (with Golden Spear)
August 12, 2010
Regulatory
June 2010 Drug Safety Labeling Changes: 28 Medical Product Labels with changes
The MedWatch June 2010 Drug Safety Labeling Changes posting includes 28 products with safety labeling changes to the following sections: BOXED WARNING, CONTRAINDICATIONS, WARNINGS, PRECAUTIONS, ADVERSE REACTIONS, PATIENT PACKAGE INSERT, and MEDICATION GUIDE.
August 4, 2010
Traceability/Serialization
Nutec Systems announces track-and-trace solution
Nutec Systems, Inc. introduces its next-generation track-and-trace solutions at Pack Expo 2010., which address several layers of track-and-trace requirements to assist companies in complying with expected FDA requirements.
August 4, 2010
Home
Label Technology Hires Sales Executive
Label Technology, Inc. today announced the addition of Robert Holt as a sales representative for their pressure sensitive label and flexible packaging product lines.
July 22, 2010
Regulatory
Arava (leflunomide): Boxed Warning - Risk of Severe Liver Injury
AUDIENCE: Rheumatology, Family Practice
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
Home
Fuwei Films Announces a New BOPET Patent for Heat Shrinkage Film
Fuwei Films (Holdings) Co. Limited (Nasdaq: FFHL) (“Fuwei” or “the Company”), a manufacturer and distributor of high-quality BOPET plastic films located in China, today announced that Fuwei Films (Shandong) Co., Ltd. (“Fuwei Shandong”), the Company’s operating subsidiary, has applied for a new BOPET films patent for heat shrinkage film which has been reviewed by the State Intellectual Property Office (SIPO) of China.
July 13, 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
Hp 19406 Pi Serialization 1
Regulatory
Tamiflu: Counterfeit Product Sold on Internet
Fraudulent product is dangerous to patients allergic to penicillin.
July 7, 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
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