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The medical device industry recorded solid performance in 2008, but regulatory and financial uncertainty make expert predictions about the year to come less definitive.
An MPO Staff Report
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In the second article from our two-part series, large contract manufacturing firms outline the advantages they can offer medical device OEMs.
Michael Barbella
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As firms compete in an increasingly global market, consultants and service providers offer a cost-effective solution for regulatory checks and balances.
Mark Crawford
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Packaging, sterilization and validation requirements all matter when developing a new device.
Garrett Douglas
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An industry expert shares tips and useful data for developing a quality-systems approach for conducting medical device clinical trials.
Susan M. Rockwell
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