The US-based multinational technology company approached Freyr for a Regulatory Intelligence (RI) report to understand the global Regulatory landscape and the specific regulations applied to their medical devices in various countries.
Freyr offered extensive support to the client in Regulatory Due-diligence and RI reporting. Freyr’s medical device experts have conducted thorough research using global Regulatory databases, collated pertinent data, and identified the merits and demerits of predicate devices in the target markets.
Decode how Freyr acknowledged the customer’s request and achieved 100% accuracy in furnishing a detailed RI report. Download the proven case.
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