Advena are the only consultancy team you need to bring your medical device through the ever changing regulatory hurdles to approval.As specialists in simplifying regulatory compliance for small and medium-sized enterprises, our consultancy services are tailored to your needs at competitive cost-effective rates. We provide expertise for the full medical device regulatory approval cycle.
Our aim is to simplify the regulation process, giving you full confidence you will be compliant with the regulations.
Advena can provide
Regulatory strategy analysis
Creation of technical documentation
Gap assessments to current UK/EU/US medical device requirements
Bespoke UK/EU/US Medical Device Regulatory Training