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Regulatory strategies and submissions for novel Class II and Class II medical devices.
Beratung für Hersteller von Medizinprodukten - Qualitätsmanagement (QM) nach ISO 13485 und CE-Zertifizierung von Medizinprodukten und In-vitro-Diagnostika.
Freyr provides End-to-End Post Brexit regulatory support for Pharma, Medical Devices, Cosmetics and Food Supplements manufacturers who are willing to market their products in...
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...