MEDICAL DEVICE REGULATORY AFFAIRS & QUALITY ASSURANCE EXCLUSIVITY
Clarvin has a consultant team focused exclusively on Regulatory Affairs and Quality Assurance for Medical Devices. We support our clients with all questions and aspects of Regulatory Affairs and Quality Assurance.
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.
Clarvin’s main goals are to assist clients with Medical Device Regulatory compliance, contribute to make new and innovative medical devices globally available to patients and shorten time-to-market by offering the best medical device expertise.