TD diagnosis before submission
Reconcile your business with your regulatory challenges
A step ahead in your monitoring
QMS AUDIT
An objective and shared perspecive on your organization
Firefighter missions
Count on Nexialist to stand by your side, holding the fire hose, and extinguishing regulatory fires
Clinical evaluation
The synthesis of your clinical data: a cornerstone in demonstrating the performance and safety of your medical device
Electrical safety
No more fear of getting shocked, nexialist secures your regulatory meter
Technical documentation
A clear and complete dossier to obtain your ultimate goal: the CE mark
Design & Development
Obtain a relevant methodology to master a simplified and operational design
Process validation
Your turnkey validation solution, optimized and compliant
Post-Market Surveillance
Demonstrate the safety and performance of your medical device throughout its lifecycle
Due diligence
Make informed decisions by assessing the regulatory health of your business