Enterprise

NoxReg for Enterprise

GxP-ready regulatory intelligence for large pharma and CRO organisations

Why Enterprise

Built for regulated environments from day one

PSMF Documentation

Receive a complete system description document to include NoxReg in your Pharmacovigilance System Master File (GVP Module I compliant).

Data Processing Agreement

GDPR-compliant DPA available immediately. Sub-processor list provided. SCCs in place with all data processors.

Vendor Qualification Support

GxP vendor audit questionnaire responses, functional specification, and validation support documentation provided on request.

Audit Trail & AI Logs

Complete AI generation logs (model version, prompt version, timestamp, output hash) available for 21 CFR Part 11 and EU Annex 11 compliance needs.

Compliance Matrix

What's included at each tier

RequirementStarterProEnterprise
GDPR DPAOn requestOn requestIncluded
PSMF System Description
Vendor Audit Pack
AI Generation Logs
21 CFR Part 11 Audit Trail
Dedicated support
Custom agency monitoring
Team seats15Unlimited

Enterprise pricing

Custom pricing for your organisation

Enterprise

Custom pricing

Typically €1,200–€5,000/month depending on team size and compliance requirements.

Contact us for a quote

Get in touch

Talk to the enterprise team

We typically respond within 1 business day.

We typically respond within 1 business day. For urgent enquiries: enterprise@noxreg.com