Freyr announced the launch of new medical devices regulatory services designed to provide a focused, market-driven approach to ensure compliance with global regulatory requirements. The new service offers an effective regulatory strategy to medical device companies to gain competitive edge in meeting the regulatory requirements.
In addition, Freyr provides end-to-end services starting from device classification to market approval which includes appointing legal representative and offering guidance in attaining certifications like QMS etc.
Freyr will assist in navigating across any regulatory issues and offers a path to approval across multiple jurisdictions through implementations of a strategic plan in registering the device for different agencies which makes the approval process easier.
Freyr’s specialized services will enable the device companies efficiently address the increased scrutiny from national regulatory agencies while minimizing downstream risks.
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