MedReg AI

MedReg AI Pricing

Pricing

Start with a free analysis. Scale as your compliance needs grow.

Starter

$79
$49 / month
For startups and small regulatory teams.
3 free reports included

Includes

  • 3 gap analysis reports per month
  • Medical devices: EU MDR and FDA 510(k)
  • Supplements: DSHEA basics
  • Up to 10 documents per project
  • Basic compliance scoring
  • PDF report export
  • Email support
Most Popular

Professional

$299
$199 / month
For teams managing multiple product types.
Best value for regulatory teams

Everything in Starter, plus

  • 15 gap analysis reports per month
  • All device pathways (MDR, IVDR, 510k, PMA, De Novo)
  • Full pharma support (NDA, ANDA, IND)
  • Complete supplement compliance (DSHEA, cGMP, NDI)
  • Unlimited document uploads
  • Advanced semantic search
  • Priority support (5 users)

Enterprise

$799
$499 / month
For large organizations with complex portfolios.
Custom solutions available

Everything in Professional, plus

  • Unlimited gap analysis reports
  • Custom regulation templates
  • Multi-jurisdictional analysis
  • API access for integration
  • SSO and audit logs
  • Dedicated account manager
  • Unlimited team members
  • Custom onboarding

Frequently Asked Questions

Common questions about MedReg AI

Have more questions? Contact our team

Client Testimonials

See how MedReg AI is transforming regulatory compliance across the life sciences industry.

DS

Dr. Sarah Chen

VP Regulatory Affairs, Global MedTech

MedReg AI reduced our EU MDR gap analysis from 3 weeks to 2 days. The AI findings are remarkably accurate and saved hundreds of hours of cross-referencing.

MT

Michael Torres

Director of RA, PharmaCorp

We used MedReg AI for our NDA submission preparation and identified critical gaps in our clinical documentation that manual review missed.

DE

Dr. Emma Williams

Chief Quality Officer, NutraScience

For dietary supplement compliance, nothing else comes close. The DSHEA and cGMP analysis is comprehensive and the recommendations are actionable.

JP

James Park

Regulatory Consultant

I recommend MedReg AI to all my clients across devices, drugs, and supplements. It provides regulatory expertise available around the clock.

DL

Dr. Lisa Anderson

CEO, BioMed Startup

As a startup, we couldn't afford a large RA team. MedReg AI gave us enterprise-level compliance capabilities at a fraction of the cost.

RK

Robert Kim

SVP Quality and Regulatory, OrthoTech

The 510(k) analysis identified predicate device gaps early in our development cycle. We received clearance without a single additional information request.