Get a 360 view of global regulatory intelligence with ARC360
Seamus Kearney at the Belfast Docks Collecting Award
At ARC we’re known as the go to for regulatory consultancy in the IVD industry but we can’t be available for all of our clients 24/7. So, we decided to channel our expertise and experience into our new digital tool which means you can find answers to questions which are critical to your clinical trial planning.
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 and functionality on the horizon as we continue on our mission to help advance the global precision medicine community together.
ARC360 is available on an annual subscription basis with two plan options; Enterprise, which is targeted to large corporates, offers unlimited global access and unlimited profiles and the Regular plan which includes the customers’ choice of country sites and is more suited to the individual consultant or smaller biotech.
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.
