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.
Company’s Keywords:
in vitro diagnostic device, ivdr, medical device, mdr, qms, qsr, ivdd, regulatory affairs, quality assurance, mdd, iso13485
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