By Daniel R. Matlis The Food and Drug Administration (FDA) announced that it has asked pharmaceutical companies to confirm or repeat all pharmacokinetic studies conducted […]
How Soon Can You Get Me That 6 Year Old Data? Read More »
FOR IMMEDIATE RELEASE Contact: Monica Malave Director, Marketing & Communications mmalave@axendia.com Yardley, PA, October 24, 2006 — Axendia, a trusted advisor to
Axendia Joins Forces with Microsoft to Strengthen BioIT Alliance Read More »
Source: Microsoft Corp. Yesterday, at Microsoft’s biotechnology Executive Forum, Microsoft announced the initiation of the BioIT Alliance’s second proof of concept, called the Biomarkers Project,
Can Microsoft Accelerate the Pace of Drug Discovery and Development? Read More »
On February 26, 2004, the FDA published its final rule on “Bar Code Label Requirements for Human Drug Products and Biological Products”. According to the
A Bar-Code In The Hand Is Worth Two RFID Tags In The Bush Read More »
The U.S. Food and Drug Administration (FDA) yesterday approved the AbioCor®, the world’s first completely self-contained, implantable Replacement Heart. This approval provides patients suffering from
FDA Approves First Implantable Replacement Heart Read More »
On August 3, 2006 MRO Software announced that it has agreed to be acquired by IBM. So, what the impact on Life-Sciences Customers? I think
The impact of IBM’s Acquisition of MRO Software on the Life-Sciences Market Read More »
I recently read an article on the Free Software Foundation’s Website entitled “Regulatory compliance is no reason to lock up users” The author states that
Can I make your pacemaker software run faster? Read More »
By Daniel R. Matlis It’s 3:00 AM and your newborn baby wakes up crying. You want to go back to sleep, but his circadian rhythm
I Lost the Cure for the Common Cold! Read More »
By Daniel R. Matlis In his recent InformationWeek article entitled “Let The UBS Trial Be A Warning To You” Mitch Wagner covers the trial against
Are Post-it Notes Security's Worst Enemy? Read More »
By Daniel R. Matlis BearingPoint announced today that it will provide services to help pharmaceutical and healthcare organizations implement SAFE (“Signatures and Authentication For Everyone”)
BearingPoint Joins SAFE’s Vendor Partner Program Read More »
by Daniel R. Matlis In a long awaited move, the FDA announced on Friday June 9th, that it will fully implement regulations related to the
FDA Task Force Report Recommends e-Pedigree in Distribution and Addresses RFID Issues Read More »
By Daniel R. Matlis This is an excerpt of my recently published article in Medical Product Outsourcing. Medical device companies have been implementing manufacturing information
Want to Buy a Bridge? The Promise of Service-Oriented Architecture Read More »
