Advena are the only consultancy team you need to bring your In-Vitro Diagnostic Regulation (IVD) 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 IVD regulatory approval cycle.
In-Vitro Diagnostic (IDV) Consultancy Advena can provide:
Regulatory strategy analysis
Device classification
Creation of technical documentation
Gap assessments to current UK/EU/US IVD requirements
Bespoke UK/EU/US IVD Regulatory Training
