Clarvin AB is a consultancy firm specializing in Medical Device Regulatory Affairs and Quality Assurance. Established in 2019, the company provides tailored strategic guidance to ensure regulatory compliance with EU and US medical device regulations. The team at Clarvin is dedicated to offering comprehensive support, addressing all aspects of Regulatory Affairs and Quality Assurance to deliver value to clients within the Health Care and Medical Devices industries. While specific details regarding the headquarter location and recent investment are not available, the company's core focus on navigating the complexities of medical device regulations positions it as an intriguing prospect for potential investors. With the increasing demand for regulatory expertise in the healthcare sector, Clarvin AB presents an opportunity for venture capital firms seeking to back innovative solutions in this niche.
Clarvin AB
Medical Device Regulatory Affairs & Quality assurance consultants
Sweden
2-10 employees
Health Care, Medical Devices
General Information
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Sweden Market
Health Care
About Clarvin AB
Taxonomy: Medical Device, Regulatory Affairs, EU Regulations, US Regulations, MDD, MDR, IVDD, IVDR, ISO13485, In Vitro Diagnostic Device, QMS, QSR
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