Priced for the
pharmacy you run,
not a generic tier.

Every 503A compounding pharmacy has a different compliance footprint — different license types, chapter obligations, team sizes, and inspection histories. Your pricing should reflect that.

Why we don't publish a price list

A single-location sterile compounding pharmacy with two pharmacists has very different compliance obligations than a multi-site non-sterile operation with twelve staff. A tiered pricing page would either overcharge you for things you don't need, or leave you guessing whether critical features are included. We'd rather take 30 minutes to understand your specific situation and give you a number that's actually accurate.

What goes into your quote.

We look at three things. Nothing more.

01

Your Compliance Scope

Which USP chapters apply to your practice — 795, 797, 800, or a combination — drives the depth of your obligation calendar and attestation workflows.

02

Number of Locations

Single-site pharmacies and multi-location groups have different coordination needs. We scale accordingly, with consolidated oversight across all sites for groups.

03

Team Size

Attestations, competency tracking, and role-based dashboards scale with your staff count. We right-size your plan to your actual headcount — not a worst-case ceiling.

Everything in the QMS plan.

CRAVE launches with one plan: QMS. It covers the full compliance program for 503A compounding pharmacies across USP 795, 797, and 800. Your price scales with team size and number of locations — not with which features you can access.

Continuous Readiness
  • Live compliance score across all applicable USP chapters
  • Predictive gap detection before deadlines hit
  • Chapter-by-chapter obligation calendar
  • Daily readiness dashboard for owners and compliance officers
Attestation & Workflows
  • Automated, role-based attestation routing
  • Deadline-aware notifications — no manual chasing
  • ESIGN/UETA-compliant e-signatures on every attestation
  • Full historical attestation trail, tamper-evident
Regulatory Intelligence
  • Automatic USP chapter change alerts
  • Gap mapping when chapters are revised
  • State Board regulation overlays by license and jurisdiction
  • DEA obligation tracking integrated
Evidence & Inspection Readiness
  • One-click inspector evidence package generation
  • Centralized SOP library with full version history
  • Staff competency records — garbing, media fills, BUD
  • Environmental monitoring logs, always current
Setup & Support
  • Guided onboarding — most pharmacies live in under a week
  • No IT department required
  • Dedicated support from compliance-literate team members
  • In-app documentation and USP reference library
Security & Compliance
  • Role-based access controls for every team member
  • Full audit trail on all platform actions
  • SOC 2-aligned data security practices
  • Data encrypted in transit and at rest
No setup fees
One plan at launch — no tier complexity
Cancel with 30 days notice
Annual & monthly options available

Expanding the platform.

These modules are in active development and will be available as add-ons to the QMS plan. Early access customers will have input on feature scope and rollout timing.

In Development

Additional Facility

Consolidated compliance oversight across multiple locations — shared SOP library, site-specific readiness scores, and cross-facility inspection packages.

  • Per-location compliance dashboards
  • Cross-site staff competency tracking
  • Unified inspection evidence packages
In Development

Compounding Operations

Full compounding record management layer — master formulation records, BUD assignments, batch-level documentation, ingredient lot tracking, and recall workflows.

  • Master formulation records (MFRs)
  • BUD calculation and assignment
  • Ingredient lot traceability and recall support
In Development

Pharmacy Law Database

State-by-state compounding shipping rules, jurisdiction comparison tools, and real-time change alerts — built for pharmacies operating across state lines.

  • Cross-state shipping rule lookup
  • "Can I ship this?" guided query flow
  • Legislation change alerts by jurisdiction

What happens when you reach out.

Three steps from first contact to a pharmacy that craves its next audit.

30-Minute Discovery Call

We learn your compliance scope — which USP chapters apply, your license type and state, team size, and current documentation workflow. No pitch, no pressure. Just a real conversation about your obligations.

Live Platform Walkthrough

We walk through CRAVE against your specific obligations — your chapters, your staff structure, your inspection history. You'll see exactly how your compliance score would look, how attestations would route, and what an evidence package for your pharmacy would include.

A Quote Built for You

Based on your scope and team, we'll give you a specific number — not a range. If it's not the right fit, we'll tell you that too. Most pharmacies are onboarded and live within a week of signing.

Have questions before you're ready for a demo?

We've answered the most common ones — from how long onboarding takes to whether CRAVE fits hospital in-house compounding operations.

Browse the FAQ

Thirty minutes to know exactly what it costs and exactly what you get.

No tiers, no guessing, no generic demo. Just a real walkthrough of your pharmacy's obligations and a price that reflects them.

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