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ARC
United Kingdom
Приєднався 1 лип 2020
ARC are a specialist Regulatory & Clinical Research Consulting Company and IVD/CDx CRO. Our mission is to support companies, from the world’s top pharmaceutical and biotech leaders to medical start-ups, in helping find kinder treatments and guiding them as they bring new medical discoveries to market.
We plan to use this channel to share who we are and what we do and any precision medicine industry insights. We do hope you will like and subscribe to keep updated with everything ARC.
We plan to use this channel to share who we are and what we do and any precision medicine industry insights. We do hope you will like and subscribe to keep updated with everything ARC.
ARC Regulatory Services Osaka 2024
ARC delivers expert solutions to the precision medicine and in vitro diagnostic (IVD) medical device sectors.
ARC’s mission is clear: 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.
Our team of IVD and companion diagnostic (CDx) regulatory experts support pharmaceutical and biotech R&D companies in their quest to find kinder, more effective patient treatments.
We integrate with existing teams and other stakeholders, guiding you through complex overlapping regulations for investigational devices used in clinical research, reducing time-to-market of new CDx devices and corresponding therapies.
ARC’s mission is clear: 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.
Our team of IVD and companion diagnostic (CDx) regulatory experts support pharmaceutical and biotech R&D companies in their quest to find kinder, more effective patient treatments.
We integrate with existing teams and other stakeholders, guiding you through complex overlapping regulations for investigational devices used in clinical research, reducing time-to-market of new CDx devices and corresponding therapies.
Переглядів: 41
Відео
Why work at ARC in Northern Ireland?
Переглядів 22Рік тому
At ARC, we're passionate about supporting the advancement of high quality biomarker testing in precision medicine research and the full service research outsourcing for in vitro diagnostic (IVD) medical device validation. Our work on more than 30 precision medicine and IVD programmes across oncology, auto immune and cardiac therapy biomarkers has helped to deliver high-quality, robust clinical ...
Introducing ARC Regulatory
Переглядів 36Рік тому
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 discov...
Welcome to the ARC360 Regulatory Navigator
Переглядів 19Рік тому
ARC360 Regulatory Navigator - Our regulatory database of over 40 Central Laboratory and Sample Collection Site country requirements for IVD/CDx clinical performance/validation studies. Implementing clinical trial assays and candidate companion diagnostics in global precision medicine studies can be complex and time intensive with ever-changing IVD regulations. Since its first publication in 201...
Introducing ARC for China Trials Conference
Переглядів 273 роки тому
Want to understand more about ARC? Here we introduce what we're all about, who we work with and what we do it all for, a summary of our unique brand proposition and purpose.
Introducing ARC360
Переглядів 1543 роки тому
ARC360 acts as your 24/7 regulatory consultant with a 360 view of the implications of regulation to each role in the partner process and all of the key tasks to feature into your planning so you have a realistic, compliant plan that helps you avoid any of the unforeseen obstacles encountered without regulatory insight. What’s more, we’ve just got started! ARC360 has even more exciting features ...