Mediteq Forum is a network of knowledge for manufacturers, suppliers, users, consultants
and distributors that handle medical devices in their daily work. The network
focuses on questions regarding quality and regulatory requirements (regulatory affairs)
for medical devices and systems.
The aim is to create an arena for discussions and exchange of experiences between
If your organization is not at a member, please send your application to email@example.com
Registration and program for upcoming activities:
Mediteq Forum is proud to invite you to participate in an extensive and highly interactive Lead Auditor Training course for ISO 13485:2016 in Gothenburg in August 2019. The course is IRCA certified and Philip Byrne from the IRCA approved training partner Irish Quality Centre (IQC) will be our trainer during the five days.
Mediteq Forum Erfarenhetsutbyte 25 april 2019. Utvärdering av biokompabilitet. Read more