Casus Consulting

medical devices

About

Casus Consulting is a European Authorized Representative, UK Responsible Person, and Swiss Authorized Representative for medical devices, including software, implantable, IVDs, custom-made devices, and more. In addition to representation, Casus provides CE and UKCA Marking consulting services to manufacturers entering the market in the EU, United Kingdom, and Switzerland. With over 15 years of industry experience, the Casus Consulting team can provide tailored solutions to address each company's unique regulatory needs. Our core value systems are to work collaboratively with clients and foster long-term partnerships; unwavering transparency in pricing, communication, and service timing; and to provide Director level support, to ensure high-quality service and the full benefit of our knowledge and experience.

Technologies

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Keywords

medical equipment manufacturing services swissmedic updates ivdr classification medical devices regulatory calendar regulatory resources regulatory project management quality assurance b2b device registration services regulatory affairs ivdr compliance market entry support conformity assessment healthcare regulatory documentation global device registration post-market surveillance device compliance regulatory updates regulatory liaison eu authorized representative market snapshot analysis compliance management clinical evaluation eudamed registration uk responsible person regulatory consulting device lifecycle management

Location

3800 North Lamar Boulevard, Austin, Texas, United States, 78756

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