Together with our partners, we offer full-service solutions. We have extensive medical device experience within Quality, Regulatory and Clinical Affairs, and we are dedicated to support you – from idea to market.
There are no off-the-shelf, one-size-fits-all solutions when it comes to compliance services. We provide customized strategic solutions based on our clients’ prerequisites and special needs.
Clarvin has extensive experience with EU, US and rest of the world regulations. We create value for our clients by providing customized global strategic input to the companies’ regulatory compliance scheme.
We are your QA/RA expert partner focusing exclusively on medical device Regulatory Affairs and Quality Assurance. Together we support and guide you with every aspects of the compliance process.
Don’t miss out!On 10-11 November, Devicia’s COO, Birgitta Larsson will once again deliver in a training course hosted by Läkemedelsakademin. Seize the opportunity to participate in an extension course on Clinical Evaluation and Clinical Investigation for Medical...