30/06/2021 Other Services
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.
Freyr provides United Kingdom Responsible Person (UKRP) services to foreign medical device manufacturers in product registration and market entry in t...
Operon Strategist offers comprehensive design and development documentation services to ensure your medical device complies with international regulat...
To register a medical device for manufacture, submit an application to the CDSCO together with the necessary documentation, which includes device deta...
Ensure your medical devices meet European standards with CE Marking. Stay compliant and gain market access across the EU. Maven is a regulatory consul...
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