Hello device manufacturers! Planning to enter new markets? Freyr is your trusted regulatory partner, offering tailored support from concept to post-market. We conduct Initial Risk Analysis, provide Market Insights, and craft Regulatory Strategies. Our services include Design Verification, Risk Management, Regulatory Submissions (EU CE marking, UKCA marking), and Global Market Access. Post-launch, we handle Post-Market Surveillance, Clinical Follow-up, Technical File Maintenance, and more. With over 380 clients and a thousand projects, trust Freyr to manage your regulatory complexities while you focus on patient care. Subscribe for regulatory insights and solutions!
Негізгі бет Comprehensive lifecycle support for medical devices
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