May 2002 Newsletter

This newsletter list items recently added to the web site as of May 17, 2002. It serves as an easy reference to find new items that may be of interest to you.
Note: Some links in older newsletters may no longer work.

What’s New

FDA:  Exemptions, Variances, and Alternate Forms of Adverse Event Reporting for Medical Devices

Manufacturers, importers, and user facilities can request an exemption or variance from any or all of the medical device reporting requirements in 21 CFR Part 803.  Read more:

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