Certificate in Medical Device Regulations for Quality Professionals
-- ViewingNowThe Certificate in Medical Device Regulations for Quality Professionals is a comprehensive course designed to empower quality professionals in the medical device industry. This program highlights the importance of regulatory compliance and quality systems, enabling learners to excel in their careers and drive success in their organizations.
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Medical Device Regulations Overview
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Understanding Quality System Regulation (QSR)
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ISO 13485: Medical Devices - Quality Management Systems
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Design Controls and Risk Management
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Change Management and Complaint Handling
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Medical Device Reporting and Adverse Event Management
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Clinical Data Management and Post-Market Surveillance
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Audit and Inspection Preparation
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Regulatory Affairs and Submissions for Medical Devices
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EntryRequirements
- BasicUnderstandingSubject
- ProficiencyEnglish
- ComputerInternetAccess
- BasicComputerSkills
- DedicationCompleteCourse
NoPriorQualifications
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- NotAccreditedRecognized
- NotRegulatedAuthorized
- ComplementaryFormalQualifications
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- ThreeFourHoursPerWeek
- EarlyCertificateDelivery
- OpenEnrollmentStartAnytime
- TwoThreeHoursPerWeek
- RegularCertificateDelivery
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