Plans & Pricing

Regulatory intelligence,
built for MedTech teams

From a solo regulatory consultant to a global portfolio team — GORA AI scales with your ambition. Start free. Upgrade when you need to.

Annual plans billed yearly. Prices in GBP, exc. VAT.

Starter
Free
 

Explore GORA AI with no commitment. Ideal for early-stage MedTech founders and students.

Get started free
What's included
  • 1 cardiovascular product
  • 3 regulatory markets
  • Basic requirements checklist
  • Regulatory map overview
  • PDF & Markdown export
  • AI regulatory assistant
  • Portfolio mode
  • Timeline & Gantt planning
  • Document repository
  • Team workspace
Team
£799/month
 

For RA teams managing multiple programmes across global markets with collaborative workflows.

Start free trial
Everything in Professional, plus
  • Up to 15 products
  • 5 user seats
  • Unlimited AI assistant queries
  • Team workspace & activity logs
  • OEM & Private Label analysis
  • Comparison table across all markets
  • Priority email support
  • Video onboarding session
  • API access
  • Custom regulatory frameworks
  • SSO / enterprise security
Enterprise
Custom
 

Tailored for large MedTech companies managing extensive global portfolios with enterprise-grade security requirements.

Talk to us
Everything in Team, plus
  • Unlimited products & markets
  • Unlimited user seats
  • API access for system integration
  • Custom regulatory framework configuration
  • SSO (SAML, OIDC) & audit logs
  • Dedicated regulatory advisor (10 hrs/month)
  • 99.9% uptime SLA
  • White-label option
  • Custom data residency (EU / UK)
  • Procurement & legal support

Compare all plans

Every feature, side by side.

Feature Starter Professional Team Enterprise
Core Platform
Products1515Unlimited
Regulatory markets3161616 + custom
User seats115Unlimited
Regulatory map
Requirements checklistsBasicFullFullFull + custom
Cost estimates per step
AI & Intelligence
AI regulatory assistant100/monthUnlimitedUnlimited
Source freshness tracking
Classification rationale
Market comparison table
Dossier & Documents
Document templates3 templatesAll templatesAll templatesAll + custom
PDF & Markdown export
Digital signatures
Document repository
Collaboration & Workflow
Portfolio mode
Timeline & Gantt planning
Team workspace
OEM / Private Label analysis
Activity logs & audit trail
Enterprise & Security
API access
SSO (SAML / OIDC)
Custom data residency
Dedicated advisor10 hrs/month
SLA guarantee99.9% uptime
Support
Support channelCommunityEmailPriority email + videoDedicated
Response timeCommunity3 business days1 business day4 hours

Frequently asked questions

Everything you need to know about GORA AI plans.

Yes — Professional and Team plans both include a 14-day free trial with no credit card required. You get full access to every feature so you can evaluate GORA AI against a real submission project before committing.
Absolutely. You can upgrade, downgrade, or cancel at any time from your account settings. Upgrades take effect immediately; downgrades take effect at the next billing cycle. Annual plans can be upgraded mid-year with prorated credit applied.
All cost estimates are sourced from publicly available official fee schedules (FDA Federal Register, TGA fee summaries, Health Canada published rates, SFDA fee guides, etc.) and are current as of the source check date shown against each item. We recommend always verifying final fees directly with the relevant authority before budgeting, as government fees are updated periodically.
GORA AI currently focuses on cardiovascular medical devices including coronary stents, PTCA balloons, drug-coated balloons, structural heart devices, atherectomy systems, heart failure devices, and imaging catheters. Support for additional therapeutic areas — including neurology, orthopaedics, and IVDs — is on our roadmap. Enterprise customers can request custom device configuration ahead of the general release.
No — and we're upfront about that. GORA AI accelerates your regulatory strategy by surfacing the right frameworks, checklists, costs, and timelines instantly. It handles the 80% of preparation that is well-established and repeatable. The remaining 20% — including device-specific clinical strategy, notified body negotiations, and country-specific nuance — still benefits from experienced RA counsel. Enterprise plans include dedicated advisor hours for exactly this purpose.
All data is encrypted in transit (TLS 1.3) and at rest (AES-256). We do not share your regulatory data with third parties, and your product configurations and dossier notes are private to your account. Enterprise customers can request EU or UK data residency. We are working towards ISO 27001 certification.
Yes — we offer a 40% discount on Professional plans for pre-revenue MedTech startups (validated by Companies House or equivalent), and free Professional access for accredited academic research groups working on medical device projects. Contact us via the form below to apply.

Ready to streamline your regulatory strategy?

Tell us about your project and we'll recommend the right plan — or set up a personalised walkthrough of the platform with our team.

  • 14-day free trial, no credit card needed
  • Onboarding call included for Team & Enterprise
  • Startup discount available on request
  • Response within 1 business day
  • UK-based team, GDPR-compliant

We'll respond within 1 business day. No spam, ever.

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Thank you — we've received your enquiry.

Expect a reply from the GORA AI team within 1 business day.