BSI The Netherlands (2797) is a leading full scope Notified Body designated under the IVDR and MDR. We are also a full scope UK Approved Body (0086) assessing medical devices against UK legislation. We review your IVD medical device to ensure conformity against the releva...
Medicines, medical equipment and medical items are subject to registration with the State Register of the Ukrainian Healthcare Ministry. Ukrainian exemption letters = explanatory letters on obligatory products certification in Ukraine The exemption letter is a document stating that the products are not su...
acting as an authorized representative of the EU, performs quality system inspections to assess the degree of conformity to prescribed relevant regulatory requirements of Good
Dr. Duccio Neri,co-founder and Executive Chairman of Philogen, commented:"We are excited that our new manufacturing facility is now poised for supplying life-saving medicines to patients who are in need. This achievement has been possible thanks to multi-million euros investments to construct the ...
(EMA) GMP certificate, following that from China National Accreditation Service for Conformity Assessment (CNAS) and China Inspection Body and Laboratory Mandatory Approval (CMA). This marks a great step for the company to be one of few third-party biosafety testing providers certified...
SONCAP Conformity Assessment Process Leno is a trusted partner to the Nigerian government. Our mandate covers the physical inspection, sampling and testing of goods at laboratories accredited as per ISO 17025. To assess the conformity of a shipment, the verification of conformity process will follow ...