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NMPB CMi

CMi/R/03/03, Issue 2, Amendment 1

ضوابط ادخال الهبات/ المنح من حكومات الدول والمنظمات العالمية
Sudanالمجلس القومي للأدوية والسموم / وزارة الصحة الاتحاديةRegistrationCurrentness under review
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

CMi/R/03/03, Issue 2, Amendment 1 is the official NMPB identifier for “ضوابط ادخال الهبات/ المنح من حكومات الدول والمنظمات العالمية”. CMi/R/03/03, Issue 2, Amendment 1 is the official identifier NMPB uses for this instrument.

Instrument
CMi
Full name
CMi/R/03/03, Issue 2, Amendment 1
Category
Registration
Source links
Source publication
Arabic
Linked source text; confirm the publisher, publication details and any later amendment or consolidated version.
Readable HTML
1 language version
Direct citations can link to a specific article or section by appending its fragment identifier.
Dates
Published
—
Effective
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Each version has stable passage anchors for direct citations and highlighting. The readable text is generated from an authority source and does not replace the legally controlling publication.

About this regulation

ضوابط ادخال الهبات/ المنح من حكومات الدول والمنظمات العالمية

Complete three-page Arabic controlled copy for donations from governments and international organisations, with all original page images and a transcription checked against the visible originals. The footer identifies issue 2 dated 2020/01/02 and amendment 1 dated 2022/08/01; its printed expiry is literally 2023/01/2. Currentness remains unverified because that controlled-copy date has passed, while the authority still publishes a corresponding undated HTML body. This is not proof of either a renewed controlled version or legal repeal. Covers preliminary approval of donated medicines and medical supplies, new and refurbished devices, consumables and all eight clearance-document requirements plus terminal matching and stamping clauses. New devices require operating/maintenance manuals, consumables, accessories and an EC/FDA certificate or registration in an approved regulatory jurisdiction; refurbished devices require preliminary technical-committee approval. Consumables require at least six months’ remaining shelf life on arrival. No legal publication or commencement date is inferred from document-control fields. A verified current version, approved-country applicability and later instruments remain under review.

CMi/R/03/03, Issue 2, Amendment 1 is the official identifier NMPB uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.