Choose Your Plan



Suitable for small consulting companies and CRO's or small biopharma (12 month minimum suscription)

  • Access up to 10x Country-specific Requirements

  • Up to 3x Central Laboratory Sites




Unlimited access to all information. Suitable for pharma/IVD companies opening clinical sites across the EU and other jurisdictions for precision medicine trials. Contact us for a voucher code if you are an existing ARC Regulatory customer. (12 month minimum suscription)

  • Unlimited Country-specific Requirements

  • Access all Central Laboratory Sites


The Plans Explained

Benefits Regular Enterprise
Single source of regulatory information
Global Clinical Development Planning Tool
Supports rapid decision making to accelerate clinical site set up
Always up to date with the latest regulatory information and community insights
Compliance built in
Supports planning of the least burdensome approach to your trial
Access requirements for ethical opinion
Understand device safety requirements in global markets
Content access for Central Laboratory Locations 10 Unlimited
Access information for Sample collection sites internationally 3 Unlimited
5 hours worth of ARC360 SME consulting support per month
*Please note that suscription autorenewal will be apply unless cancelled before 30days of renewal date.*
  • Reduce study start up time by up to a third

  • Your 24/7 CDx Regulatory Consultant

  • Tailor your reports to specific trial scenarios

  • Learn from a community of your peers in the precision medicine industry