Freyr provides medical device regulatory services in RoW Market that span across medical device registration, notification and local representation services for successful and compliant market entry of products.
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Freyr provides UKRP services and Key takeaways for foreign medical device manufacturers to comply with MHRA regulations and market entry of the product in the UK.
Freyr acts as a United Kingdom Responsible Person (UKRP) for medical device manufacturers on their behalf for product registration and UK market entry
Freyr provides United Kingdom Responsible Person (UKRP) services to foreign medical device manufacturers in product registration and market entry in the UK and acts as a single point of contact in the Country for liaison with Regulatory Agency.