Targeted and accurate knowledge of your competitors and their products is a key component in understanding the market landscape of your medical device.

Depending on your needs, we can gather and analyze information on your competitors, predicate devices, and other market factors. Outsourcing such investigations to Devicia ensures no traceability back to you, as our client.



Our team consists of experienced medical writers and information search specialists with PhD’s in multiple fields. Devicia is a member of a variety of committees and trade organizations, both in the EU and the US, and provide our clients with industry perspective and first-hand advice, always from a global viewpoint.

Our services includes:

  • Extensive searches
  • IP-related searches
  • Benchmark identification
  • Identification of ongoing clinical studies within your field
  • Review of FDA 510(k) applications
  • Competitors’ regulatory strategy e.g. MDD to MDR transitions
  • Monitoring of competitors ongoing clinical activities
  • Untraceable investigations


Whether you have questions regarding regulations, clinical strategies, educations or need help with an audit, you are always more than welcome to contact us.

Our ecosystem for full-service medical device compliance

We are your full-service medical device partners. Together we offer unique expertise regarding Quality Assurance, Regulatory Affairs, Clinical Affairs, Biological Evaluations & Toxicology.