At Samaraz Investments Limited, we specialize in providing end-to-end regulatory services for medical device manufacturers looking to enter the African market, especially Zambia and Southern Africa.
Our services include:
✅ Product Registration with ZAMRA (Zambia Medicines Regulatory Authority)
✅ In-Country Validation & Laboratory Evaluation with the Ministry of Health
✅ Clinical Trials & Protocol Management with certified investigators
✅ Regulatory Consultancy to ensure fast-track market entry
✅ Dossier Preparation, Document Submission & Manufacturer Representation
We bridge manufacturers with key health regulatory institutions, ensuring your products meet all local compliance requirements for importation and distribution.
Backed by a team of experts and partnerships with state institutions, Samaraz ensures your innovations reach the patients who need them—quickly and lawfully.
Contact us today to start your registration or clinical trial journey in Africa's emerging healthcare markets.
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