Day

January 16, 1997
a. The reason for changes made to the CNC software programs was not documented nor signed off by a designated individual. b. When the CNC software is changed, the previous versions are overwritten or lost, thus making traceability of the software’s evolution impossible. 4. Failure to conduct processing control operations in a manner designed to...
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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:  https://www.fda.gov/medical-devices/medical-device-reporting-mdr-how-report-medical-device-problems/exemptions-variances-and-alternate-forms-adverse-event-reporting-medical-devices

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