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Regulatory Affairs & Pharmaceutical Licensing
Published: 2026-09-29
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Editorial Team
We guide medicines and health products through the regulatory process in Sudan, preparing registration files and following them up with the authorities until approval.
Our specialized regulatory team possesses comprehensive insight into the requirements of the National Medicines and Poisons Board (NMPB) and the Ministry of Health, delivering seamless approvals with zero procedural delays.
Core areas include:
- Registration of human pharmaceuticals, biopharmaceuticals, nutritional supplements, and cosmetics.
- Licensing and GMP accreditation of international manufacturing facilities and quality control laboratories.
- Post-marketing regulatory maintenance, dossier variations, and pharmacovigilance follow-up.
⚡ Key Features & Highlights
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Product Registration
Comprehensive dossier submission and persistent follow-up until license issuance.
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Pharmaceutical Laboratories
Accreditation and statutory verification for analytical and testing laboratories.
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Factory Licensing
GMP audit facilitation and official registration of overseas pharmaceutical plants.
Have Questions About This?
Get in touch with our team for more information or assistance.