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Friday, January 12, 2018
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What is Process Validation Report | 21CFR11 Compliance Checklist 2018
January 11, 2018 at 9am to January 12, 2018 at 6pm – Germany Course "Validation and 21 CFR Part 11 Compliance of Computer Systems" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completio… Organized by NetZealous DBA as GlobalCompliancePanel | Type: regulatory, and, compliance, seminars
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The Value of a Human Factors Program
January 12, 2018 from 10am to 11am – Fremont Overview: This webinar will explain the implementation of ISO 62366 and the regulatory expectations discussed in the 2016 FDA Guidance for a compliant human factors/ usability program. Why should you… Organized by Event Manager | Type: online
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Clinical Data Systems Regulated by FDA
January 12, 2018 from 10am to 11:30am – Fremont Overview: Companies engaged in the conduct of human clinical trials must adhere to specific government regulatory requirements.Certain documents, content and images related to a clinical trial must b… Organized by Event Manager | Type: online
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