Mediteq is a team of consultants who helps and guides you in the regulatory landscape of requirements for medical device development, market access and CE-marking.
Mediteq is a personal, professional and customer oriented consulting firm that always have clear goals, an open mindset and a long-term perspective in our deliverables.
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.
Uppskattat erfarenhetsutbyte - Utvärdering av biokompatibilitet Read more