Regulación del Etiquetado de Dispositivos Médicos: Avanzado
June 25, 2026 2026-06-26 3:24Regulación del Etiquetado de Dispositivos Médicos: Avanzado
Regulación del Etiquetado de Dispositivos Médicos: Avanzado
Move from foundations to applied labeling regulation — author SOPs under ISO 13485, audit real labels against ISO 20417 and ISO 15223-1, defend a RACT, and integrate labeling controls into the QMS CAPA loop.
Recommended prerequisite: completion of the Introductorio level for this training, or relevant professional experience subject to Aleph University review.
The Avanzado level of the Aleph Regulación del Etiquetado de Dispositivos Médicos course track is for professionals who already have the labeling vocabulary covered at orientation depth and need to develop the applied skills the medical-device industry expects: authoring a Standard Operating Procedure under ISO 13485 using a structured auditable format (three-part header, sign-off, version control, flowchart); auditing a real medical-device label against ISO 20417:2021 and 21 CFR 801 Subpart A; applying ISO 15223-1 symbol conventions including the explanation-in-labeling rule; constructing a Risk Assessment Categorization Tool (RACT) for a labeling-related risk, scoring severity and probability independently, defending residual-risk acceptability with mitigation language grounded in clause; and integrating the CAPA loop and the complaint-to-recall escalation that govern labeling defects in operational practice.
This 32-hour Curso de Certificación Profesional builds directly on the 16-hour Introductorio level (`RAQ-514-I`). It does not repeat the labeling-vocabulary orientation. Where the Introductorio level identifies ISO 13485, the Avanzado level authors a labeling SOP within its discipline. Where the Introductorio level identifies ISO 20417 and ISO 15223, the Avanzado level audits a real label against them. Where the Introductorio level identifies the CAPA framework, the Avanzado level walks the complete escalation path: complaint → CAPA → labeling change → 510(k) amendment → recall classification. The course culminates in a final integrative assessment that exercises the participant’s command of the framework on a labeling scenario.
Graduates of the Avanzado course are positioned for senior applied work in Asuntos Regulatorios and Quality roles with labeling responsibility, in consulting firms supporting clients on labeling remediation, in UDI compliance teams, and in QMS audit programs. The SOP, the label audit, and the RACT produced during the course are portfolio-grade artifacts that demonstrate working command of the labeling discipline.
Los participantes que cumplan los requisitos de finalización del curso reciben un Certificado de Finalización emitido por Aleph University.
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