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Perspectives

INBETWEEN Testing Alliance LLC Announces Medical Device Membership Drive

Jan 10 | News

DENVER, CO – Now medical device compliance officers and quality assurance teams will have reliable access to competitive predicate device samples required for FDA product clearance, thanks to the newly launched INBETWEEN Testing Alliance™. A privately held company...

A proactive approach to healthcare

A proactive approach to healthcare

Oct 26 2011 | Articles

We’ve cured cancer. Well...not quite, but according to some, early detection will eradicate deadly diseases. This was one of many fascinating topics covered at the 2011 Imec Tech Forum.

Perspectives on 2010 Year in Review

Perspectives on 2010 Year in Review

May 10 2011 | Perspectives

What was the most significant headline in the medical device manufacturing industry in 2010?

Perspectives on Time to Market—Part 3

Perspectives on Time to Market—Part 3

Jan 31 2011 | Perspectives

For your area of the industry, what is your best recommendation for getting a medical device to market faster?

Perspectives on Time to Market—Part 2

Perspectives on Time to Market—Part 2

Jan 4 2011 | Perspectives

For your area of the industry, what is your best recommendation for getting a medical device to market faster?

Perspectives on Time to Market—Part 1

Perspectives on Time to Market—Part 1

Dec 16 2010 | Perspectives

For your area of the industry, what is your best recommendation for getting a medical device to market faster? Heather Dunn, Director of Engineering, CIRTEC Medical Systems: CIRTEC Medical Systems is commonly requested to perform accelerated product developments for our clients. The CIRTEC approach in those situations involves a few key tactics.

Perspectives on Implantables

Perspectives on Implantables

Sep 21 2010 | Perspectives

What advances specific to implantable devices will the medical device community see in the next five to ten years?

Perspectives on the FDA Review Process

Perspectives on the FDA Review Process

Aug 17 2010 | Perspectives

Should the FDA review process be more relaxed in favor of faster review times at the expense of potentially greater impact to the well-being of patients when a device does fail?

Perspectives on Global Design

Perspectives on Global Design

Jul 7 2010 | Perspectives

For your area of the industry, what is the most significant consideration when designing a device for use both domestically and internationally?

Perspectives on Medical Electronics

Perspectives on Medical Electronics

Apr 8 2010 | Perspectives

The role of electronics in medical devices has evolved tremendously over the last several decades and continues to integrate into more products as the industry moves forward.

Perspectives on New Materials, Part II

Perspectives on New Materials, Part II

Mar 23 2010 | Perspectives

New developments in material technology are critical to innovations across all industries, including medical device technology. Therefore, it is crucial for designers to stay abreast of the most recent advances that could benefit their upcoming products.

Perspectives on New Materials, Part I

Perspectives on New Materials, Part I

Mar 23 2010 | Perspectives

New developments in material technology are critical to innovations across all industries, including medical device technology. Therefore, it is crucial for designers to stay abreast of the most recent advances that could benefit their upcoming products.

Perspectives on Lean Manufacturing, Part II

Perspectives on Lean Manufacturing, Part II

Jan 22 2010 | Perspectives

Lean manufacturing can help companies eliminate waste, reduce costs, and improve timeliness.

Perspectives on Lean Manufacturing, Part I

Perspectives on Lean Manufacturing, Part I

Jan 22 2010 | Perspectives

Lean manufacturing can help companies eliminate waste, reduce costs, and improve timeliness.

Perspectives on the FDA UDI Rule, Part II

Perspectives on the FDA UDI Rule, Part II

Dec 2 2009 | Perspectives

The FDA's upcoming UDI rule will impact all medical device manufacturers. To what degree, however, will vary from company to company, based on what systems and technologies are already in place.

Perspectives on the FDA UDI Rule, Part I

Perspectives on the FDA UDI Rule, Part I

Dec 2 2009 | Perspectives

The FDA's upcoming UDI rule will impact all medical device manufacturers. To what degree, however, will vary from company to company, based on what systems and technologies are already in place.

Perspectives on Manufacturing Technologies, Part IV

Perspectives on Manufacturing Technologies, Part IV

Oct 5 2009 | Perspectives

The capabilities of manufacturers are growing to enable the fabrication of components that are extremely tiny, very complex, and incredibly intricate. These advances are leading to medical devices that could not have been developed just a few years ago.

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