Free Sale Certificate and Apostille Pack for Medical Device Exports
Quick answer: A free sale certificate proves that a device may be sold freely in the country of manufacture, and an apostille...
Leer artículoCE, ISO 13485, FDA, MDR, IEC 60601, RoHS, REACH, UDI, Venta Libre, Apostilla y notificación de vigilancia para equipos médicos.
Quick answer: A free sale certificate proves that a device may be sold freely in the country of manufacture, and an apostille...
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The EU MDR transition has set a phased deadline that runs past 2027, which means a device placed on the EU market...
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The UAE operates a two-track system for medical device oversight: a federal track under the Ministry of Health and Prevention (MOHAP) that...
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Tanzania is one of East Africa’s most active medical device import markets, and its regulator — the Tanzania Medicines and Medical Devices...
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Nigeria NAFDAC Requirements for Medical Devices Nigeria is the largest medical device market in West Africa by population, and every imported device...
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Certificate Package for African Tenders: CE, ISO, Legalisation and Apostille On paper, an equipment tender is won on price. In practice, a...
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Kenya Medical Device Registration: Pharmacy and Poisons Board If you want to sell a medical device in Kenya, you need to register...
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Post-Market Surveillance Plans for Distributors Post-market surveillance is not a compliance box; it is the ongoing process of watching a device in...
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The price of a surgical light or operating table from China is rarely the most expensive part of the deal. The cost...
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Etiquetado e instrucciones de uso: conceptos básicos del MDR para productos sanitarios. En la Unión Europea, un producto sanitario no es legal poner en el mercado...
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