Freyr Medical Devices

Pharma / Medical

Randburg, South Africa

Freyr Provides End-to-end Medical device regulatory consulting support for medical devices and IVD companies that span across device registration, classification, and market access of products in compliance with Country-specific regulations across the globe.

As a proven medical device Regulatory consulting firm, for nearly a decade, Freyr has been setting the industry standards in assisting Medical Device and IVD companies worldwide for end-to-end Regulatory needs and product registration.

With an enormous experience in areas such as Medical device consulting, IVD regulatory consulting, Medical device compliance, and many more – Freyr brings to you the best in class industry experts for addressing all your regulatory requirements.

• Clinical Evaluation Report
• Global Regulatory Intelligence
• Medical Device Labeling and Review
• Staff Augmentation
• Regulatory Strategy and Approach
• Translation Support
• Device Technical File Publishing
• Design History File

As a medical device consulting and IVD Regulatory consulting organization, Freyr is uniquely positioned to deploy best vertical/divisional in-house experts to provide the best Regulatory approach, specifically for combination product portfolio companies. The customized nature of Freyr services is synchronized keeping in mind our customers’ growth strategy and product portfolio.

Freyr offers a robust combination of technology and Regulatory expertise to ensure product continuity, label compliance, and data quality. We are committed to partnering with companies by providing strategic guidance as they develop, advance and innovate devices. Here is a brief track record of Freyr.