Proceso de Desarrollo de Productos Médicos: Avanzado

Proceso de Desarrollo de Productos Médicos: Avanzado

Product Development — Applied Stage-Gate Plan, Applied 21 CFR §820.30 Controles de Diseño, ICH Q8 QbD, V&V Planning, and Capstone Development Plan

Proceso de Desarrollo de Productos Médicos: Avanzado

Move from foundations to applied medical-product development — author a stage-gate plan, apply 21 CFR §820.30 Controles de Diseño and ICH Q8 QbD, integrate risk management, plan V&V, select a regulatory pathway, and deliver a complete medical-product development plan.

RAQ-600-AAvanzado32 horasCertificado de Finalización

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Proceso de Desarrollo de Productos Médicos
FormatoCurso de Certificación Profesional
NivelAvanzado
Duración32 horas
IdiomaInglés
CertificadoCertificado de Finalización — Aleph University
Full course trackIntroductorio (16 h) + Avanzado (32 h) = 48 horas
Requisito previo / Preparación recomendada

Recommended prerequisite: completion of the Introductorio level for this training, or relevant professional experience subject to Aleph University review.

Descripción general

The Avanzado level of the Aleph Proceso de Desarrollo de Productos Médicos course track is for professionals who already have the stage-gate, Controles de Diseño, and ICH Q8 vocabulary covered at orientation depth and need to develop the applied skills the regulated industries expect: authoring a stage-gate plan with explicit deliverables and decision criteria at each gate; applying 21 CFR §820.30 Controles de Diseño to a chosen medical-product program (Design Input, Design Output, Design Review, Design Verification, Design Validation, Design Transfer, Design Changes, Design History File); applying ICH Q8 Quality by Design with critical quality attributes and a control strategy; integrating ISO 14971 (devices) and ICH Q9 (pharmaceuticals) risk management decisions across the stage gates; planning verification and validation aligned with 21 CFR §820.30(f)–(g) for devices and analytical-method validation for pharmaceuticals; selecting a regulatory pathway with a defensible rationale; analyzing real recall cases for root-cause patterns tied to development-process failures; and authoring a complete medical-product development plan as a portfolio-grade deliverable.

This 32-hour Curso de Certificación Profesional builds directly on the 16-hour Introductorio level (`RAQ-600-I`). It does not repeat the stage-gate, Controles de Diseño, or ICH Q8 vocabulary orientation. Where the Introductorio level identifies stage-gate methodology, the Avanzado level authors a stage-gate plan for a chosen medical-product program. Where the Introductorio level identifies the FDA Controles de Diseño clauses, the Avanzado level applies them to a chosen program with documented Design Input, Design Output, and Design Review artifacts. The course is organized around a chosen-program cumulative deliverable arc — the participant selects a medical-product program in Module 1, builds development-plan content on it across Modules 2 through 8, and integrates everything into a complete medical-product development plan in the Module 9 capstone course exercise.

Lo que aprenderás
Author a stage-gate plan with explicit deliverables and decision criteria at each gate.
Apply 21 CFR §820.30 Controles de Diseño to a chosen medical-product program.
Apply ICH Q8 Quality by Design to a chosen pharmaceutical program with critical quality attributes and a control strategy.
Integrate ISO 14971 (devices) and ICH Q9 (pharmaceuticals) risk management decisions across stage gates.
Plan verification and validation aligned with 21 CFR §820.30(f)–(g) for devices and analytical-method validation for pharmaceuticals.
Select a regulatory pathway (FDA, EU MDR / IVDR, ICH-aligned pharmaceutical pathways) with a defensible rationale.
Analyze real recall cases for root-cause patterns tied to development-process failures.
Author a complete medical-product development plan integrating all of the above on a chosen program.
course topics & modules
Relevancia profesional

Graduates of the Avanzado course are positioned for senior applied work in product-development leadership, regulatory strategy, R&D program management, and quality program leadership at medical-device, pharmaceutical, and combination-product manufacturers; at medical-product startups; and at consultancies serving manufacturers on product-development planning. The authored medical-product development plan produced during the course is a portfolio-grade artifact.

Certificado de Finalización

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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