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April 19, 2016
Soapbox

For Cost Cutting Measures, Look to Business Process Automation

By Steve Smith
No Comments

Today’s business operations environment demands faster, more tangible returns.

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Michael Lohan, IDA Ireland
March 15, 2016
Michael Lohan, IDA Ireland
Soapbox

Recruiting Tomorrow’s Medtech Workforce: Insights from Ireland

By Michael Lohan
2 Comments

Cultivating fresh thinking and continual adaptation is key.

Continue reading →

David Amor, Medgineering
February 12, 2016
David Amor, Medgineering
Soapbox

Evaluate a Company’s Regulatory and Quality ‘Health’ Before Investing

By David Amor
4 Comments

Why regulatory and quality due-diligence is often overlooked.

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February 4, 2016
Soapbox

Want to Be a Medical Device Entrepreneur?

By Scott Phillips
14 Comments

Shift the odds in your favor.

Continue reading →

Mika Javanainen, M-Files Corp., Hybrid cloud for medical device manufacturers
January 29, 2016
Mika Javanainen, M-Files Corp., Hybrid cloud for medical device manufacturers
Soapbox

The Big Data and Big Content Disconnect for Medical Device Manufacturers

By Mika Javanainen
No Comments

Take a metadata-driven approach to information management.

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Nicholas Daniell, Sunrise Labs
November 19, 2015
Nicholas Daniell, Sunrise Labs
Soapbox

Robust Security Planning Requires Change in Mindset

By Nicholas Daniell
4 Comments

Product architects are challenged to address security throughout the device lifecycle.

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Engineering World Health, Biomedical trainers
November 16, 2015
Engineering World Health, Biomedical trainers
Soapbox

Lack of Operational Medtech Equipment in Developing World

By Leslie Calman, Ph.D., Jessica Baker
No Comments

Having trained biomedical equipment technicians in developing regions can help, but lack of funding is perpetuating a dire situation.

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Jon Speer, Greenlight.guru
November 12, 2015
Jon Speer, Greenlight.guru
Soapbox

7 Steps to Respond to FDA 483 Inspection Observations

By Jon Speer
2 Comments

Inspections are inevitable. If you receive 483s, follow these tips to quickly and adequately respond to the agency.

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Nicole Littman, Quorum Consulting
October 8, 2015
Nicole Littman, Quorum Consulting
Soapbox

CMS Reveals Rationale for NTAP Decisions in Rule Making

By Nicole Littmann
1 Comment

What can we learn about how new technologies become eligible for additional payment?

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Jon Speer, Greenlight.guru
September 28, 2015
Jon Speer, Greenlight.guru
Soapbox

4 Reasons Your Risk Management Approach is Wrong

By Jon Speer
2 Comments

Risk Management is the single most important topic impacting the medical device industry today.

Continue reading →

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