Legal and de facto: Office 320, Kudryavsky descent 7, 04053 Kyiv
See on the map Monday - Thursday 9.00 - 18.00 Friday 9.00-17.00, without break
Feedback
Journal “Laboratory” No. 06/2020 The text of the article is available only in Ukrainian
Read moreManufacturers operating under the (EU) 2017/745 Medical Device Regulation (MDR) and (EU) 2017/746 In Vitro Diagnostic Regulation (IVDR) are required to utilise the European Medical Device Nomenclature (EMDN) for regulatory submissions, device registration in EUDAMED, and sampling. To support consistent and compliant application, MedTech Europe released a practical guide for the use of the […]
Read moreThePharmaMedia The first independent pharmaceutical business portal. The text of the article is available only in Ukrainian
Read moreOr find the answer here
*All fields are required