About
Clarvin has a consultant team focused exclusively on Regulatory Affairs and Quality Assurance for Medical Devices. Clarvin has extensive experience with EU and US medical device regulations and we create value for our clients by providing customized strategic input to the company´s regulatory compliance scheme. We support our clients with all questions and aspects of Regulatory Affairs and Quality Assurance.
Technologies
Outlook
Microsoft Office 365
Google Tag Manager
Varnish
Apache
reCAPTCHA
WordPress.org
Mobile Friendly
Google Font API
Basis
Keywords
medical device
in vitro diagnostic device
mdr
qms
ivdd
qsr
quality assurance
ivdr
mdd
iso13485
regulatory affairs
medical equipment manufacturing
clinical investigation
usability study
regulatory strategy
clinical evidence for medical device software
post-market surveillance
ce marking
medical writing
prrc
other scientific and technical consulting services
technical documentation
b2b
regulatory guidance
mdr/ivdr transition
regulatory consulting
uk responsible person
eu authorized representative
biocompatibility & toxicology
regulatory framework adaptation
Company Information
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Employees 10
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Founded 2011
Location
12B Riddargatan, Stockholm, Stockholm County, Sweden, 114 35
