Certified Professional in Biomedical Device Certification
-- ViewingNowCertified Professional in Biomedical Device Certification (CPBDC) equips professionals with in-depth knowledge of medical device regulations. This certification is ideal for quality assurance, regulatory affairs, and clinical engineering professionals.
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- Quality System Regulations (QSR) and ISO 13485
- Risk Management (e.g., ISO 14971)
- Design Controls
- Regulatory Affairs and Submissions (e.g., 510(k), PMA)
- Labeling and Packaging
- Biocompatibility
- Electrical Safety
- Good Manufacturing Practices (GMP)
- Post-Market Surveillance
- Human Factors Engineering
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Career Role Description Biomedical Device Certification Specialist (Primary: Certification, Biomedical Device; Secondary: Regulatory Affairs, Quality) Ensures compliance with regulatory standards for biomedical devices, including ISO 13485 and MDSAP.
A crucial role in maintaining product safety and market access.
Senior Biomedical Engineer - Certification (Primary: Biomedical Engineer, Certification; Secondary: Design, Validation) Leads the certification process for new and existing devices.
Possesses deep technical expertise and regulatory knowledge.
Regulatory Affairs Manager - Biomedical Devices (Primary: Regulatory Affairs, Biomedical Devices; Secondary: Compliance, Certification) Manages all aspects of regulatory compliance, including submissions for certification and maintenance of registrations.
A key liaison between the company and regulatory bodies.
Quality Assurance Auditor - Medical Devices (Primary: Quality Assurance, Medical Devices; Secondary: ISO 13485, Certification Audits) Conducts internal and external audits to ensure that quality management systems meet relevant standards for device certification and compliance.
EntryRequirements
- BasicUnderstandingSubject
- ProficiencyEnglish
- ComputerInternetAccess
- BasicComputerSkills
- DedicationCompleteCourse
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- ThreeFourHoursPerWeek
- EarlyCertificateDelivery
- OpenEnrollmentStartAnytime
- TwoThreeHoursPerWeek
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