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...
Baca ArtikelCE, ISO 13485, FDA, MDR, IEC 60601, RoHS, REACH, UDI, Penjualan Bebas, Apostille, dan pelaporan kewaspadaan untuk peralatan medis.
Quick answer: A free sale certificate proves that a device may be sold freely in the country of manufacture, and an apostille...
Baca Artikel
The EU MDR transition has set a phased deadline that runs past 2027, which means a device placed on the EU market...
Baca Artikel
The UAE operates a two-track system for medical device oversight: a federal track under the Ministry of Health and Prevention (MOHAP) that...
Baca Artikel
Tanzania is one of East Africa’s most active medical device import markets, and its regulator — the Tanzania Medicines and Medical Devices...
Baca Artikel
Nigeria NAFDAC Requirements for Medical Devices Nigeria is the largest medical device market in West Africa by population, and every imported device...
Baca Artikel
Certificate Package for African Tenders: CE, ISO, Legalisation and Apostille On paper, an equipment tender is won on price. In practice, a...
Baca Artikel
Kenya Medical Device Registration: Pharmacy and Poisons Board If you want to sell a medical device in Kenya, you need to register...
Baca Artikel
Post-Market Surveillance Plans for Distributors Post-market surveillance is not a compliance box; it is the ongoing process of watching a device in...
Baca Artikel
The price of a surgical light or operating table from China is rarely the most expensive part of the deal. The cost...
Baca Artikel
Pelabelan dan Petunjuk Penggunaan: Dasar-dasar MDR untuk Alat Kesehatan Di Uni Eropa, alat kesehatan tidak legal untuk ditempatkan...
Baca Artikel