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Wednesday, May 16, 2007
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Army Looking for Collaborators—on Device Development
There are many ways to fund product development. One that doesn't get much press is to collaborate with the U.S. Army. After you read the May issue of MD&DI, it won't be a secret any longer.
The U.S. Army Medical Research and Materiel Command (USAMRMC) is a major contributor of funds and manpower to medical device development. The USAMRMC is the command through which the Army determines what it requires to meet the medical and health needs of its soldiers. If the technology to address a need is available, USAMRMC purchases it. If it is not available, USAMRMC finds universities and companies with which to collaborate on development, shepherds the resulting products through clinical trials and FDA approval, and purchases them for use on the battlefield and elsewhere. It enters into a variety of development contracts with firms and universities.
In most cases, if the USAMRMC is going to help fund the development of a product, the device needs to be of use to conditions on the battlefield. But it wants to hear any and all proposals.
If you are interested in developing a relationship with USAMRMC, one of the people you should get to know is William Howell, its first principal assistant for acquisition. Howell is one of the highest-ranking civilians in the Army and oversees USAMRMC's efforts, from proof of concept through FDA approval and purchasing. Howell is the subject of the Q&A feature in the May issue of MD&DI. In the interview, he explains how collaboration with the USAMRMC works, what kinds of technologies the Army is looking for, and how device companies can go about submitting an idea.
As medical devices and the challenges of funding their development get more complex, firms are going to need to come up with different ways to get their products developed and launched. For some, collaborating with the Army may be the answer. The Defense Department budget is getting bigger, while some other sources of funding are getting smaller. So, MD&DI's readers should pay attention to what Howell has to say.
Erik Swain
erik.swain@cancom.com


Plastics
Trends in Device Design: Implications for Materials Selection
By Clare Frissora
OEMs can address a number of trends, such as miniaturization and environmental regulation, through careful plastics selection.
Adhesives
Adhesive Makers Add Conductivity to the Mix
By William Leventon
New adhesive formulations enable OEMs to develop adhesives that conduct electricity while they connect components.
Testing
Using Chemical Characterization to Show Equivalency
By David Albert and Amy Hoffmann
Establishing device biocompatibility requires OEMs to fully understand a material’s properties. Here are some tests that can help OEMs along.
Clinical Trials
Best of Both Worlds: SOPs for Device Trials in Europe, Part 1
By Nancy J. Stark
Creating a hybrid clinical trial procedure that incorporates both the ICH-GCPs and ISO 14155 can help smooth the path to successful European trials.
Software
Sales and Software: Highlighting the Customer Experience
By Bruce Cameron
Customer relationship management systems can help OEMs make the most of their interactions with current and potential customers.
Injection Molding
Saddling Up CIM for Medical Devices
By Travis Ayers
Ceramic injection molding is increasingly being considered for microsized parts that must withstand wear.
More from this issue of MD&DI
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In today's world, it's no surprise that device companies are trying to develop products that will help protect the public in the event of a biologic disaster. To that end, FDA has approved two filtering faceplate respirators that help reduce exposure to airborne germs in the case of a public health emergency.
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