INVIMA DocumentINVIMA semantic-standard reporting instructions V6 (July 2026)
Currentness under review. Whether this instrument remains applicable is under review. Consult the later instruments and source context below before relying on it.
Instructivo para el manejo de la plataforma de reporte de estándar semántico —versión 6 is published by Instituto Nacional de Vigilancia de Medicamentos y Alimentos. This document is identified by its title; no separate official document code is recorded.
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Instructivo para el manejo de la plataforma de reporte de estándar semántico —versión 6
Complete 53-page official INVIMA instructions for the semantic-standard reporting platform, printed version 6 and Bogotá, D.C., July 2026. The original explicitly covers medical devices and in vitro diagnostic reagents and retains separate templates, registration-holder and authorized-reporter roles, manufacturer/brand/reference data fields, report verification and payment workflow. This complete captured expression is distinct from the separate 17-page standard/UDI guide already held in the system. Original page images govern the unchanged native search layer, including image-only cover and back-cover institutional/contact lettering absent from native extraction. It does not establish product-registration modification requirements, approval of holder transfers, current fees or any answered-question outcome. Source-only preservation; no facts, fees, timings, bindings or question status changes.
This document is identified by its title; no separate official document code is recorded. Always confirm the current consolidated text and transition provisions with the official source before filing.