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Page 39 of 44 Pages |
Beninese demand changes, as Boni marks 100 days in office
Topix
- Sunday, August 13, 2006
More than 100 days after t he inauguration of Yayi Thomas Boni as Benin President, his compatriots are already asking for the political and economic changes which the former banker promised on his
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EXPERTS ASK FDA TO CLARIFY, SIMPLIFY BAYESIAN STATISTICS GUIDANCE
FDAnews
- Sunday, August 13, 2006
The FDA recently received comments on its "Guidance for the Use of Bayesian Statistics in Medical Device Clinical Trials ? Draft Guidance for Industry and FDA Staff," issued May
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MEDTRONIC ENTERS INTO $40 MILLION SETTLEMENT WITH DOJ OVER WHISTLEBLOWER ALLEGATIONS
FDAnews
- Sunday, August 13, 2006
The Department of Justice (DOJ) and Medtronic announced July 18 the firm will pay the government $40 million to settle civil allegations the firm's Sofamor Danek division paid kickbacks to healthcare professionals (HCPs) inducing them to use Medtronic's spinal
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FDA APPROVES ABBOTT'S AUTOMATED DIAGNOSTIC FOR HEPATITIS B SURFACE ANTIGEN
FDAnews
- Sunday, August 13, 2006
The FDA July 18 said it had approved the first fully automated product that both screens and confirms tests for hepatitis B surface antigen
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FDA ISSUES OPHTHALMIC PANEL MEETING SUMMARY; SPECIFIES SAFETY CONCERNS REGARDING VISIONCARE EYE DEVICE
FDAnews
- Sunday, August 13, 2006
The FDA July 18 provided an explanation of the safety concerns of its Ophthalmic Devices Panel in recommending against approval for VisionCare's Implantable Miniature Telescope
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FDA APPROVES FUJI COMPUTED RADIOGRAPHY MAMMOGRAPHY SUITE
FDAnews
- Sunday, August 13, 2006
The FDA announced it has approved the Fuji Computed Radiography Mammography (FCRm) manufactured by FujiFilm Medical System
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ABBOTT, MEDINOL SETTLING PATENT SUIT AGAINST ABBOTT STENT
FDAnews
- Sunday, August 13, 2006
Abbott Laboratories Inc. is finalizing a patent infringement case settlement with Israeli company Medinol Ltd. that could free Abbott's Xience drug-coated stent medical device from an entanglement as Abbott works to bring the product to the U.S.
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SMITH & NEPHEW RECEIVES FDA APPROVAL FOR EXOGEN 4000+* BONE HEALING SYSTEM
FDAnews
- Sunday, August 13, 2006
Smith & Nephew's Orthopaedic Trauma & Clinical Therapies division announced FDA approval for its EXOGEN 4000+* Bone Healing
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NEW RESEARCH VALIDATES INNOVATIVE DIAGNOSTIC TESTING APPROACH TO SLEEP APNEA PATIENT CARE WITHIN THE VETERANS AFFAIRS HEALTH SYSTEM
FDAnews
- Sunday, August 13, 2006
The Department of Veterans Affairs (VA) has solved a serious
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S3 INVESTMENT COMPANY SUBSIDIARY SINO UJE RECEIVES DISTRIBUTION RIGHTS TO MEDICAL DIAGNOSTIC TESTING PRODUCTS IN CHINA MARKET
FDAnews
- Sunday, August 13, 2006
S3 Investment Company, Inc., announced that subsidiary SINO UJE, Ltd. has been awarded distribution rights in China to the HandiLab line of medical diagnostic tests from Zonda Incorporated, a California-based
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World Bank's Wolfowitz hails Benin as Africa model
Topix
- Sunday, August 13, 2006
World Bank President Paul Wolfowitz praised Benin on Wednesday as a democratic example that other countries in West Africa could learn
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France: The Beginnings of Affirmative Action
Global Voices Online
- Sunday, August 13, 2006
Says (Fr) France-based Senegalese blogger Seckasysteme about the allegedly affirmative-action induced hiring and debut of Black French newsanchor Harry Roselmack on French national television: “Roselmack’s (…) professional competence and the recognition he has earned from his peers is so obvious that even the
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Full Issue in PDF Format
FDAnews
- Sunday, August 13, 2006
View the entire issue in PDF
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Medtronic Enters $40 Million Settlement Over Whistleblower Allegations
FDAnews
- Sunday, August 13, 2006
The Department of Justice (DOJ) and Medtronic announced July 18 the firm will pay the government $40 million to settle a civil suit alleging that the firm’s Sofamor Danek division paid kickbacks to healthcare professionals to induce them to use Medtronic’s spinal
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Some Doctors Cutting Back on Imaging Device Purchases Due to Proposed Cuts
FDAnews
- Sunday, August 13, 2006
Some doctors are buying fewer medical devices because of planned cuts to Medicare reimbursements for certain medical imaging services. The cuts are slated to start in January
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Greater Focus on PR Essential in Device and Diagnostics Industry
FDAnews
- Sunday, August 13, 2006
Image may not be everything, but more device and diagnostics manufacturers are working to keep theirs as positive as
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FDA: Catheter Maker Had No Premarket Clearance for Devices
FDAnews
- Sunday, August 13, 2006
Advanced Medical Systems’ Cholangio catheters were adulterated and misbranded because the company did not have the required premarket clearance from the FDA for the device, said a July 13 agency warning
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Aksys Warning Letter Adds to Company’s Troubles
FDAnews
- Sunday, August 13, 2006
The FDA sent personal hemodialysis (PHD) system maker Aksys a June 8 warning letter saying that its devices were adulterated and misbranded because the company changed its recommendation for how long patients should use the system without requesting premarket
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Despite Short-Term Costs, Guidant Acquisition Seen as Boon to Abbott
FDAnews
- Sunday, August 13, 2006
Analysts are projecting a sunny outlook for Abbott Laboratories based on 2006 second-quarter results — despite some company challenges.At first glance, the company may seem to be faring worse than it actually is, said stock market website www.SeekingAlpha.com Editor Jonathan
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FDA Calls Blood Warmer Adulterated
FDAnews
- Sunday, August 13, 2006
Gaymar Industries, which makes blood warmers, received a June 8 FDA warning letter saying it failed to keep appropriate records of complaints that some of the devices were overheating or
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