ARC Regulatory is a niche provider of global regulatory and clinical research solutions to the precision medicine and in vitro diagnostic (IVD) medical device industry. It’s mission is clear: to support companies in their quest to find kinder patient treatments and act as a friendly guide through the complex, myriad of regulatory and research requirements as these firms bring new medical discoveries to market.
ARC is a trusted partner in the global ambition to improve patient care, leveraging global expertise in delivering high quality, accelerated clinical research for biomarker diagnostics.
Headquartered in Northern Ireland, ARC's expertise spans regulatory requirements for in vitro and companion in vitro diagnostic medical devices across the major global markets, with representation in the UK, EU, UAE, North America and Asia.
ARC experts work with large and small companies alike from the world’s leading pharmaceutical and companion in vitro diagnostic companies to start-ups, excited by their new innovation and ready to take it to market. ARC remains committed to supporting the promise of precision therapies for patients worldwide.
Article written by ARC Insights
October 25, 2023
ARC Insights offers a mix of industry specific content with the aim to keep its readers informed, educated, and up to date with the latest developments, trends, and expert knowledge in the FiH translational medicine space.
