Testing Documentaiton, Val Regulatory Compliance

IQ/OQ/PQ Establishing Proven Protocols for Meeting Regulatory Compliance, Managing Testing Documentation and Improving the Overall Validaiton Process
Semptember 26-27, 2002
Hyatt Regency at Penn’s Landing
Philadelphia, PA

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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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