£1,500/month
Suitable for small consulting companies and CRO's or small biopharma
Access up to 10x Country-specific Requirements
Up to 3x Central Laboratory Sites
£4,000/month
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.
Unlimited Country-specific Requirements
Access all Central Laboratory Sites
| 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 |
| ARC360 Profile | Single | Unlimited |
| Live Support (Coming Soon) | Unlimited | |
| Access to the ARC 360 Contributor Programme |
