Risk Management for Medical Devices: Introductory

Risk Management for Medical Devices: Introductory

Risk Management — ISO 14971 Vocabulary and Process Foundations

Risk Management for Medical Devices: Introductory

Build a working foundation in medical-device risk management — ISO 14971:2019 vocabulary, the seven-phase process, and orientation to FMEA, FTA, and Hazard Analysis.

RAQ-530-IIntroductory16 hoursCertificate of Completion

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Risk Management for Medical Devices
FormatCurso de Certificación Profesional
LevelIntroductory
Duration16 hours
LanguageEnglish
CertificateCertificate of Completion — Aleph University
Full course trackIntroductory (16 h) + Advanced (32 h) = 48 hours
Prerequisite / Recommended Preparation

No se requiere ningún curso previo de Aleph.

Overview

Risk management is the discipline by which medical-device manufacturers demonstrate that their products deliver clinical benefit while keeping patient harm within acceptable limits. ISO 14971:2019 is the international standard that articulates this process — one of the few standards explicitly referenced by the FDA, EU MDR, Health Canada, and other regulators. For professionals who design, validate, register, or surveil medical devices, command of ISO 14971 is a daily professional requirement.

This 16-hour Curso de Certificación Profesional is the entry point of the Aleph Risk Management for Medical Devices course track. It introduces the ISO 14971:2019 framework: the canonical vocabulary (harm, hazard, hazardous situation, risk, severity), the seven phases of the risk-management process (Planning, Analysis, Estimation, Evaluation, Control, Residual Risk Evaluation, Production and Post-Production Monitoring), the orientation to the principal hazard-identification methodologies (Preliminary Hazard Analysis, Failure Mode and Effects Analysis, Fault Tree Analysis, Hazard and Operability Study), and an orientation to IEC 62366-1 usability engineering as it integrates with risk management.

The course prepares participants for the Advanced level (`RAQ-530-A`), where the same content is exercised at applied depth — applied FMEA and FTA, applied risk-control-hierarchy decision-making, applied residual-risk evaluation with ALARP reasoning, applied IEC 62366-1 integration, applied post-market surveillance analysis using the FDA MAUDE database, and an authored Risk Management File and Risk Management Report for a chosen device. Together the Introductory and Advanced levels form a 48-hour course track.

Lo que aprenderás
Define ISO 14971:2019 vocabulary precisely (harm, hazard, hazardous situation, risk, severity, residual risk).
Explain the ISO 14971:2019 framework and its scope across devices, SaMD, and IVDs.
Identify the seven phases of the ISO 14971 risk-management process.
Recognize the structure of a Risk Management Plan and the role of acceptability criteria and methodologies.
Distinguish top-down hazard-identification methods (Hazard Analysis) from bottom-up methods (FMEA, FTA).
Recognize the ISO 14971 risk-control hierarchy (inherent safety by design, protective measures, information for safety).
Recognize the integration between risk management and IEC 62366-1 usability engineering at orientation depth.
Articulate where the rest of the course track (Advanced level) extends each topic into applied work.
course topics & modules
Relevancia profesional

The Introductory course establishes the risk-management vocabulary the medical-device industry expects of any professional with a stake in the Risk Management File. Employers in this space include medical-device manufacturers, IVD manufacturers, consultancies serving manufacturers, and post-market surveillance teams.

Certificate of Completion

Los participantes que cumplan los requisitos de finalización del curso reciben un Certificado de Finalización emitido por Aleph University.

La finalización de los niveles Introductorio y Avanzado puede ser evaluada por Aleph University para su posible reconocimiento dentro de una ruta de posgrado aplicable, sujeto a revisión institucional y a las políticas académicas vigentes. El reconocimiento no es automático ni está garantizado.
Preguntas frecuentes
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