Generated by Meeveem AI
"Regulatory and clinical research partner for precision medicine and diagnostic device development."
ARC Regulatory supports pharmaceutical, biotech, and diagnostic companies through the complex regulatory landscape of precision medicine clinical trials. The company specialises in compliance for in vitro diagnostic (IVD) and companion diagnostic (CDx) medical devices, delivering expert regulatory affairs, clinical monitoring, quality management, and CRO services. Founded in Belfast in 2010, ARC integrates with client teams to navigate overlapping global regulations for investigational devices, reduce time to market, and ensure platinum standard clinical research that protects participant welfare while generating robust data for decision making in drug and diagnostic development.
30
Team Members
2010
Founded
Consulting
Sector
On-Site
Work Environment
A future where patient care is kind, available and precise, with all global citizens benefiting from next generation technologies and therapies.
ARC's mission is to be the preferred partner for the global precision medicine and IVD industry, supporting the development of kinder treatments and expediting the highest quality clinical research for improved patient outcomes.