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| Freyr UK Responsible Person (UKRP) - Medical Devices |
| 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. » Details |
| Operon Strategist |
| Get guidance for medical device registration like ISO 13485, ISO 15378, CE marking, CDSCO, FDA, USFDA. » Details |
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