Now accepting early access partners

The infrastructure for
medicine brands

RxForge is the all-in-one platform to launch, manage, and scale your pharmaceutical or wellness brand. Regulatory. Supply chain. Compliance. Distribution. All handled.

SOC 2 Compliant
FDA-Aligned Workflows
GMP Documentation

Trusted by 50+ medicine brand founders

NB
NovaBio
VC
VitaCore
MP
MedPrime
PS
PharmaStar
WR
WellnessRx

“RxForge cut our regulatory setup time from 6 months to 3 weeks. The compliance tooling alone saved us $40K in consultant fees. It's the infrastructure layer we didn't know we needed.”

Dr. Sarah Chen

CEO, NovaBio Supplements

Platform Capabilities

Everything you need to launch

From regulatory strategy to last-mile delivery, RxForge provides the infrastructure layer so you can focus on building great products.

Regulatory Guidance

Navigate FDA, EMA, and global regulatory frameworks with confidence. Our platform maps your product to required submissions, labeling rules, and approval pathways.

Supply Chain Management

Connect with vetted manufacturers, manage raw material sourcing, and track every batch from production to shelf — with full chain-of-custody visibility.

Compliance Tooling

Automated GMP documentation, real-time audit trails, and adverse event reporting. Stay compliant without drowning in paperwork.

Distribution Logistics

Temperature-controlled shipping, pharmacy network integration, and last-mile delivery orchestration. Get your products exactly where they need to be.

How It Works

Three steps to market

We've distilled the complex journey of bringing a medicine brand to market into a streamlined, supported process.

01

Define Your Brand

Tell us about your product — formulation, target market, regulatory jurisdiction. We build your compliance roadmap instantly.

02

Build & Validate

Our platform connects you with certified manufacturers and manages documentation, testing, and quality assurance in parallel.

03

Launch & Scale

Go to market with integrated distribution, real-time inventory tracking, and automated compliance monitoring as you grow.

Security & Compliance

Built on enterprise-grade security

AES-256 Encryption

Data encrypted at rest and in transit

SOC 2 Type II

Audited security controls and processes

FDA 21 CFR Part 11

Electronic records & signatures compliant

99.9% Uptime SLA

Enterprise-grade infrastructure reliability

GDPR Ready

Full data protection regulation compliance

Full Audit Trail

Every action logged and traceable

Why RxForge

The smarter path to market

See how RxForge compares to the traditional approaches for launching a medicine brand.

RxForge

All-in-one platform

Consultants

Traditional agencies

DIY

Do it yourself

Monthly cost
From $299/mo
$5K–$15K per engagement
"Free" + your time
Regulatory guidance
Built-in, always current
Per-project, one-time
Self-research, high risk
Supply chain management
Integrated platform
Not included
Cobbled from spreadsheets
Compliance automation
Fully automated
Manual documentation
Manual, error-prone
Distribution logistics
End-to-end
Not included
Figure it out yourself
Time to launch
Weeks, not months
3–6 months typical
6–12+ months
Ongoing monitoring
Real-time alerts
Additional retainer required
Hope for the best
Scalability
Unlimited — grows with you
Rebill for each new product
Breaks as you grow

Scroll horizontally to see full comparison

Pricing

Transparent pricing that scales

From first product launch to enterprise portfolio — choose the plan that matches your stage. Upgrade anytime as you grow.

Starter

$299/mo

For early-stage supplement and wellness brands navigating their first product launch.

Get Started
Regulatory checklist tools
Basic compliance templates
Community access
Self-serve knowledge base
Email support
Most Popular

Growth

$799/mo

For scaling brands that need end-to-end infrastructure to accelerate time-to-market.

Start Growing
Everything in Starter
Full supply chain management
Compliance automation
Distribution logistics dashboard
Priority support

Enterprise

$2,499/mo

For pharma companies and established brands requiring bespoke compliance infrastructure.

Contact Sales
Everything in Growth
Dedicated regulatory advisor
Custom integrations
White-glove onboarding
Custom reporting & analytics
SLA-backed support

Need a custom plan? Talk to our team about enterprise volumes and bespoke configurations.

Limited — First 50 Partners

Become a Founding Member

Get priority onboarding, a personalized regulatory pathway assessment, a custom launch roadmap, and lifetime founding member pricing. One-time investment for permanent advantages.

$499one-time • lifetime benefits
Claim Your Spot

Real Challenges We Solve

The problems founders face every day

These quotes represent common pain points we hear from supplement and medicine brand founders.*

We spent 8 months trying to figure out FDA labeling requirements on our own. The amount of conflicting information online is staggering — we needed a single source of truth.

Supplement Brand Founder

On the challenge of navigating regulatory requirements

Our regulatory consultant charged us $12,000 for a compliance review that took 6 weeks. And that was just for one product in one market. We knew there had to be a better way.

Wellness Brand CEO

On the cost of traditional consulting

Managing compliance documentation across three different spreadsheets, two shared drives, and email threads was a nightmare. One missed update could mean an FDA warning letter.

Nutraceutical Operations Director

On compliance documentation challenges

* Representative pain points based on conversations with supplement and medicine brand founders. Not attributed to specific individuals.

FAQ

Common questions

Everything you need to know about RxForge and getting started.

RxForge is a software infrastructure platform — we don't manufacture products, so FDA approval doesn't apply to us directly. However, our platform is built around FDA-aligned workflows and helps your brand meet FDA requirements including 21 CFR Part 111 (cGMP for dietary supplements), 21 CFR Part 11 (electronic records), and proper labeling under DSHEA. We keep our regulatory databases current so your compliance posture stays up to date.

We cover the full compliance spectrum for medicine and supplement brands: FDA regulatory guidance (cGMP, labeling, DSHEA, NDI notifications), international frameworks (EMA, Health Canada, TGA), quality management systems, adverse event reporting, supply chain documentation and chain-of-custody, and post-market surveillance. Our compliance engine monitors regulatory changes in real-time and alerts you to any impact on your products.

Yes — there are no long-term contracts. You can cancel your subscription at any time, effective at the end of your current billing period. All your data remains accessible for 30 days after cancellation so you can export anything you need. We also offer a 14-day free trial on Starter and Growth plans so you can evaluate the platform risk-free.

RxForge supports the full spectrum — from dietary supplements and wellness products to OTC medications and prescription pharmaceuticals. Our platform adapts to your regulatory jurisdiction and product category, providing the specific guidance and tooling you need whether you're launching a collagen supplement or a novel therapeutic.

Traditional regulatory consultants charge $5,000-$15,000 per engagement for a single area of expertise. RxForge provides continuous, end-to-end coverage — regulatory guidance, supply chain management, compliance automation, and distribution logistics — all in one platform. You get always-on tooling instead of occasional advice, at a fraction of the cost.

Starter and Growth customers can be fully set up within 48 hours using our guided onboarding flow. Enterprise customers receive white-glove onboarding with a dedicated account manager — including data migration, team training, and custom integration setup — typically completed within 2 weeks.

Security is foundational to everything we build. RxForge is SOC 2 Type II compliant, uses AES-256 encryption at rest and TLS 1.3 in transit, and maintains full audit trails for every action. Our infrastructure meets the data handling requirements of FDA 21 CFR Part 11 for electronic records and signatures.

Absolutely. You can upgrade at any time, and we'll prorate the difference. Downgrading takes effect at the start of your next billing cycle. All your data, configurations, and compliance records are preserved across plan changes. Many of our customers start on Starter and upgrade to Growth as they scale.

Still have questions? Reach out to our team. We're happy to help.

Early Access

Be among the first

Join a select group of founders shaping the future of medicine brand infrastructure. Early partners get priority onboarding and exclusive pricing.

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