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Offshore Risks and the Case for Re-shoring
Chris Coghlin , CEO of the Coghlin Companies
August 2, 2012
There are a number of solid reasons to bring medical device manufacturing back to the United States.   Read More »
Prototypes and Production: Benefits of a Prototype Mold for Establishing Production Mold Parameters
Vince Lomax, Vice President of Tech Mold Inc.
June 20, 2012
Choosing a prototyping method that allows the engineering team to retrieve valuable data up front can often shorten this process and optimize the design and build phases.  Read More »
Charlie Alfred and Christopher Miles, Foliage Inc.
June 4, 2012
The earliest development phases make or break a product.  Read More »
In Pursuit of Automation
Jim Stertz, Director of Quality/Technology for Lowell Inc.
January 19, 2012
A contract manufacturer shares some of his company's learning curve with implementing automation.   Read More »
Evaluating Challenges & Opportunities
MedicalDeviceNow Staff
November 29, 2011
The head of Jabil's global healthcare business provides international perspective on the medical device sector, contract manufacturing and what the year ahead may hold in store.   Read More »
Managing the Risk of Medical Device Software
Rutul Dave, Senior Project Manager, Coverity Inc.
October 6, 2011
Challenges can be being met with development testing solutions and best practices that ensure the integrity of safety-critical code bases.  Read More »
The Consumerization of Medical Products
Joel Delman
August 31, 2011
The digital health movement is quickly merging cutting-edge technologies with the growing need for medical devices that help consumers manage their care more flexibly.   Read More »
The Need for Integration in Product Design
Tim J. Morton, Product Development Technologies
August 25, 2011
When research, design implementation and production are integrated and transparent across the team, the outcome is a more successful proposition and a much more efficient development process.  Read More »
HACCP for Medical Device and Pharmaceuticals
Tim Lozier
August 3, 2011
I recently was speaking to a group of folks on the different ways to mitigate risk. While this may not seem like "exciting" dialogue, it actually provoked an interesting thought—while many organizations interpret Risk factors differen…  Read More »
Three Keys to Global Harmonization in Quality: Learning to Share
Tim Lozier
June 23, 2011
Growing up, I never was one to want to share my toys.  I wasn’t one to throw a temper tantrum and take my toys home, but I never really liked the whole concept of people touching my stuff.  Thinking back on it, it all boiled down to…  Read More »
The Big Three: Tests Every Manufacturer Needs to Know
Thor Rollins
April 14, 2011
There are myriad tests that medical device manufacturers need to be prepared to conduct on their creations in order to pass regulation requirements before they are released to the marketplace. None more important than the Cytoxicity, Sensitization,…  Read More »
Marc Bertaud
November 11, 2010
Early research may seem slow early on, but it speeds up the product development process.   Read More »
Execute & Verify: Last But Not Least
Brenda Percy
September 9, 2009
Life science organizations must keep up with the industry’s high demand for innovation by constantly changing products and processes to remain competitive.   Read More »
Managing the Total Product Life Cycle
Daniel R. Matlis, President
July 23, 2009
The changing face of medical device product development.  Read More »
A Standard Challenge
Michael Barbella
June 8, 2009
A perpetual flow of revisions to sterilization and packaging standards reveals the only true constant in the industry: change.  Read More »

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