Blogs about: Fda Related
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Webinar: How Can You Quickly Adopt Data Standards for Unique Device Identification?
Loftware is pleased to announce, as an extension of our blog, a series of educational webinars to focus on the process of meeting unique device identification requirements and the adoption of GS1 data… more →
Loftware
Webinar: How Can You Quickly Adopt Data Standards for Unique Device Identification?
svigneault wrote 1 week ago: Loftware is pleased to announce, as an extension of our blog, a series of educational webinars to fo … more →
VHA Asks FDA for Speedy UDI Decision; Inclusion of Only GS1 Standards as Single Mandatory Solution
sterling1 wrote 1 week ago: This news comes from Healthcare Purchasing News: VHA Inc. and 13 of its largest health system membe … more →
FDA Launches New 'Safe Use Initiative' to Reduce Medication Errors
Christopher Little wrote 2 weeks ago: I go to the U.S. Food and Drug Administration (FDA) website almost every day to glimpse their recent … more →
Online Videos and Presentations from 15th Global GS1 Healthcare Conference Now Available
Christopher Little wrote 1 month ago: GS1 has alerted us to the availability of online videos and presentations captured in Hong Kong in e … more →
First View of FDA UDI Regulations . . . Just Hours Away?
sterling1 wrote 1 month ago: This is a reminder of the UDI 2009 Conference that gets underway twelve hours from now, in Orlando. … more →
FDA's Jay Crowley to give UDI Keynote at Upcoming Virtual Trade Show
Christopher Little wrote 1 month ago: “The Upside of a Unique Device Identification (UDI) Mandate” is the topic of an online k … more →
In Emerging Markets, Big Pharma Pursuing 'Branded Generics' Strategy -- Still Means GS1 Barcodes On Market Compliant Labels
Christopher Little wrote 1 month ago: In this article, entitled “Major pharmaceutical companies see generics as a bridge to the futu … more →
AP Story Slams Lack of Medical Device Tracking; FDA's UDI Labeling Gets Brief Mention As Answer
Christopher Little wrote 1 month ago: The Associated Press put out a story today that’s getting a lot of traction and that’s g … more →
Oracle OpenWorld Panel Update: "Oracle, the FDA, GS1, and Loftware: Improving Supply Chain Safety and Standards"
Christopher Little wrote 1 month ago: By now you’re aware of the upcoming Oracle OpenWorld event starting October 12th in San Franc … more →
The FDA, the UDI law, GS1 and Two Pivotal Dates: 10/12/09 and 10/20/09
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Christopher Little wrote 1 month ago: Here’s a look at an email we got from GS1 Healthcare US about the upcoming UDI Conference bein … more →
GS1 to be the Standard for UDI in China
Christopher Little wrote 1 month ago: Big news: In an email today from John Roberts, Director, GS1 Healthcare US, we’re being inform … more →
'Emerging Markets' Label No Longer Applicable Says Financial Expert - But GS1 Labeling Is Still Very Applicable
Christopher Little wrote 1 month ago: In an online story from the UK’s Financial Times, writer Marko Dimitrijevic says this: The ter … more →
"Oracle, the FDA, GS1 and Loftware: Improving Supply Chain Safety and Standards" - Up-Coming OpenWorld Panel!
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Christopher Little wrote 2 months ago: Editor’s note: As an editorial decision since the inception of this blog, I’ve steered a … more →
FDA's UDI Implementation will Target Class III Devices First
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sterling1 wrote 2 months ago: I should have caught this in July when FDA NEWS posted this update from Jay Crowley, who is the Food … more →
New FDA Reporting Requirement To Make Food Safer?
svigneault wrote 2 months ago: The Food and Drug Administration on Tuesday unveiled a new electronic database where manufacturers m … more →
As Loftware Preps for Oracle OpenWorld, 11g R2 Debuts
Christopher Little wrote 2 months ago: This is the first of several planned posts about a major healthcare technology panel at Oracle OpenW … more →
FDA's Top Medical Device Regulator Quits; More Turmoil on Horizon?
sterling1 wrote 3 months ago: Medical device manufacturers are already facing some uncertainty about impending rules for device id … more →
FDA Visits Foreign Manufacturers of Medium Risk Medical Devices Once Every 27 Years
Christopher Little wrote 3 months ago: Some days I am very optimistic about the changes afoot to make the Food and Drug Administration a st … more →
Strong Food Safety Bill Working its Way Through Congress
sterling1 wrote 3 months ago: File this under, ‘It’s about time!” The US House of Representatives has passed a b … more →
