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MS/HP / ANRP Arrêté

Arrêté n°000570/MS/HP/ANRP/DVUE

Organisation et fonctionnement du Comité Technique des Essais Cliniques (CTEC)
NigerMinistère de la Santé et de l'Hygiène PubliqueClinical TrialsCurrentness under review
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Document status

Currentness under review. Whether this instrument remains applicable is under review. Consult the later instruments and source context below before relying on it.

What this code is

Arrêté n°000570/MS/HP/ANRP/DVUE is the official MS/HP / ANRP identifier for “Organisation et fonctionnement du Comité Technique des Essais Cliniques (CTEC)”. Arrêté n°000570/MS/HP/ANRP/DVUE is the official identifier MS/HP / ANRP uses for this instrument.

Instrument
Arrêté
Full name
Arrêté n°000570/MS/HP/ANRP/DVUE
Category
Clinical Trials
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Source publication
French
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About this regulation

Organisation et fonctionnement du Comité Technique des Essais Cliniques (CTEC)

Four-page implementing instrument expressly linked by Article 1 to Article 35 of Order 382 of 22 September 2025; the latter's Article 36 expressly covers in vitro diagnostic medical devices. Defines CTEC missions, composition, meetings, reporting, conflicts and confidentiality. Institutional relevance does not establish a separate general device premarket committee or IVD dossier adaptation. Signed 4 December 2025; later currentness and referenced administrative arrangements remain unverified. Duplicate Chapter II and the source heading CHPITRE III are preserved.

Arrêté n°000570/MS/HP/ANRP/DVUE is the official identifier MS/HP / ANRP uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.

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