Looking for support with medical device regulatory affairs, market access, Authorised Representative services, product registration or compliance?
Contact ALTRION Group at info@altrion-group.com.
Our international regulatory team supports medical device manufacturers across the European Union, Switzerland, the United Kingdom and South Korea.
Send us your request and we will get back to you within 24 hours.
Switzerland Headquarters
ALTRION Sagl
Swiss Authorised Representative (CH-REP)
Swiss market access, CH-REP, Swiss Importer services, Swissdamed support.
Registered office address:
Via Mulino 3
6855 Stabio
Svizzera
European Union Office
ALTRION Srl
EU Authorised Representative (EU-REP)
EU MDR & IVDR compliance, EU-REP services, Technical Documentation, PMS & PSUR.
EU MDR & IVDR compliance, EU-REP services, Technical Documentation, PMS & PSUR.
Registered office address:
Via Bocchetto, 6
20123, Milano (MI)
Italy
United Kingdom Office
ALTRION GROUP UK Ltd
UK Responsible Person (UKRP)
MDR/UKCA transition, UKRP services, MHRA registrations, and post-market support.
MDR/UKCA transition, UKRP services, MHRA registrations, and post-market support.
Registered office address:
Flat 81, Seacon Tower, 5 Hutching’s Street
London, England, E14 8JX
United Kingdom
South Korea Office
ALTRION KOREA Ltd
Korea Regulatory & Market Access Office
MFDS regulatory support, Korea market access, local representation and post-market support.
MFDS regulatory support, Korea market access, local representation and post-market support.
Registered office address:
30, Jeonpa-ro, Manan-gu, Anyang-si,
Gyeonggi-do
Republic of Korea
Service availability and contracting entity may vary depending on the applicable jurisdiction.
The relevant legal entity will always be specified in the contractual documentation.
The relevant legal entity will always be specified in the contractual documentation.