On 26 May 2021, EU Medical Device Regulation (MDR) replaced the EU’s current Medical Device Directives and while the medical devices manufacturers have largely ensured compliance with the new regulation, this change will have an impact on development of documentation related to the medical devices, translation and regulatory cycles in the EU.
Having completed two three-year certification circles, Ciklopea confirmed its status of certified quality control system with a new recertification in accordance with ISO 9001:2008 and ISO 17100:2015 (substitute to EN 15038). The supervision audit for information security management system in accordance ISO 27001:2013 was also successfully completed. The regular recertification and supervision audits were conducted […]
This type of translation services uses proxy servers to render multilingual versions of a website
Ciklopea, one of the leading LSPs (translation and localization services providers) in the Republic of Croatia and in the wider region of Southeast Europe (SEE) has joined the international Globalization and Localization Association (GALA) as a corporate member. GALA is an international nonprofit association whose member companies specialize in language services, translation services and language […]