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ABMed HO-LD-0001,

HO-LD-0001, version 1

Bonnes pratiques de revue des dossiers d’homologation
BeninAgence béninoise du Médicament et des autres produits de SantéRegistrationEffective 2025-11-03
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What this code is

HO-LD-0001, version 1 is the official ABMed identifier for “Bonnes pratiques de revue des dossiers d’homologation”. HO-LD-0001, version 1 is the official identifier ABMed uses for this instrument.

Instrument
HO-LD-0001,
Full name
HO-LD-0001, version 1
Category
Registration
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Source publication
French
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Dates
Published
—
Effective
2025-11-03
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About this regulation

Bonnes pratiques de revue des dossiers d’homologation

Complete sixteen-page official good-review-practices guideline, version 1, applied from 3 November 2025. Governs evaluation quality, conflicts of interest, confidentiality, communication and review strategy for medicines and other health products; the product definition expressly includes medical devices, laboratory reagents and diagnostic products. Covers initial applications, renewals and variations as general review practices rather than a device-specific change-classification table.

HO-LD-0001, version 1 is the official identifier ABMed uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.

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