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...
اقرأ المقالCE، ISO 13485، FDA، MDR، IEC 60601، RoHS، REACH، UDI، البيع الحر، أبوستيل، والإبلاغ عن الترصد للمعدات الطبية.
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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وضع العلامات وتعليمات الاستخدام: أساسيات لائحة الأجهزة الطبية (MDR) للأجهزة الطبية في الاتحاد الأوروبي، لا يُعد الجهاز الطبي قانونيًا لوضعه...
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