Topical Issues on Medical Devices Seminar, 14 November 2018, Helsinki
The European Union regulation on medical devices 2017/745 (MDR) requires implementation of unique identifiers on medical devices by early 2020’s. Similar Unique Device Identification system has already been implemented in the USA. The pharmaceutical industry has already experienced implementation of a comparable system, called serialization, with the EU deadline in February 2019.
Industry and regulatory experts will gather to Helsinki, Finland, to discuss topical issues in medical devices in a seminar arranged by the Pharmaceutical Information Centre on 14 November 2018.
Servicepoint’s Chief Technology Officer Iiro Jantunen, D.Sc. (Tech.), will be giving a presentation at the conference of the topic “Unique Device Identification vs. safety marking of medicinal packages”. The presentation will discuss regulations and technical implementation, comparison to experiences in the pharmaceutical industry.
Servicepoint has over 30 years of experience in the pharmaceutical and several years in medical devices industry and has done 1000 production & packaging line upgrades or new installations. Servicepoint can help you throughout the whole serialization and automation projects, from consulting and design & engineering to implementation, validation, and maintenance.
CTO, Chief Technology Officer
Servicepoint Kuopio Oy
+358 44 7868 215