PLATFORM FEATURES
RegenCompliance combines real-time scanning, AI-powered rewrites, and a living compliance library into a single platform purpose-built for healthcare marketing compliance - from regenerative medicine and med spas to dental, dermatology, weight loss, and beyond.
CORE FEATURE
The compliance scanner is the heart of RegenCompliance. Paste any marketing content into the scanner and receive an instant compliance score with line-by-line analysis of every potential FDA or FTC violation. The scanner cross-references your content against our database of over 300 active compliance rules derived from real enforcement actions, warning letters, and regulatory guidance documents.
Unlike generic grammar tools or basic keyword checkers, our scanner understands context. It knows the difference between a patient testimonial that crosses the line into an implied health claim and one that stays within compliant boundaries. It flags phrases like "FDA-approved stem cells" (there are no FDA-approved stem cell products for most orthopedic or aesthetic uses), "cures arthritis," and "reverses aging" while explaining exactly why each phrase creates regulatory risk.
Each scan produces a detailed compliance report with a numeric score from 0 to 100, a severity breakdown of all flagged items (high, medium, low risk), and specific citations to the FDA warning letter or FTC enforcement action that makes each phrase problematic. You see exactly what regulators would see, before they see it.
See the full scanner breakdownThe scanner analyzes content at the sentence level, checking each statement against FDA 21 CFR Part 1271 guidance, FTC Section 5 requirements, state medical board advertising rules, and our proprietary database of phrases flagged in real enforcement actions.
FLAGGED
"Our stem cell therapy cures knee arthritis and eliminates the need for surgery."
REWRITTEN
"Many of our patients report reduced joint discomfort and improved mobility following our regenerative protocols. Individual results vary."
AI-POWERED
Finding compliance violations is only half the problem. The real challenge is rewriting flagged content so it remains persuasive and on-brand while meeting regulatory standards. That is exactly what the AI Rewriter does. When the scanner flags a violation, the rewriter generates compliant alternative language with a single click.
The rewriter is not a generic AI text generator. It has been specifically trained on FDA and FTC enforcement language, compliant marketing examples from leading healthcare practices across all specialties, and the nuanced difference between a health claim, a structure/function claim, and a patient experience statement. It understands that "heals damaged tissue" is a drug claim that requires FDA approval, while "may support the body's natural healing processes" is a structure/function claim that carries significantly less regulatory risk.
Every rewrite comes with an explanation of why the original language was problematic and what specific regulatory principle the new language satisfies. This means your marketing team does not just get compliant copy - they learn the compliance reasoning behind each change. Over time, your team writes fewer violations because they understand the underlying rules, not just the individual corrections.
See the full rewriter breakdownKNOWLEDGE BASE
The Compliance Library is a searchable, categorized database of over 300 active compliance rules covering healthcare marketing across all practice types. Each rule includes the banned or risky phrase, a compliant alternative, a risk severity rating, and the original source - whether that is an FDA warning letter, FTC press release, CBER guidance document, or state medical board ruling.
The library is organized by treatment type (PRP, stem cells, exosomes, peptides, prolotherapy, BMAC, Wharton's jelly, dermal fillers, weight loss treatments, dental implants, chiropractic, IV therapy), by claim type (efficacy claims, cure claims, FDA status claims, testimonial claims, comparative claims), and by risk level. You can browse it like a reference manual or search for specific phrases to check before you publish.
Think of it as a living compliance manual written specifically for your industry. Healthcare attorneys charge $500 to $1,000 per hour to review marketing content. The compliance library gives your team the same reference knowledge that those attorneys use, accessible instantly and updated automatically as new enforcement actions are published.
See the full library breakdown300+
Active compliance rules
1,200+
FDA warning letters analyzed
450+
FTC enforcement actions tracked
15-30
New rules added monthly
Monitor
Our system monitors FDA.gov, FTC.gov, and state medical board websites every morning for new enforcement actions, warning letters, and guidance updates.
Analyze
New enforcement actions are analyzed to extract specific language violations, banned claims, and compliance requirements relevant to healthcare marketing - including regenerative medicine, aesthetics, dental, weight loss, and more.
Update
New rules are added to the compliance database within 24 hours. Your next scan automatically includes the updated ruleset.
Alert
Significant new enforcement actions trigger in-app alerts so your team knows immediately when the compliance landscape shifts.
ALWAYS CURRENT
Compliance is not static. The FDA issues new warning letters to healthcare practices every month. The FTC regularly updates its enforcement guidance on health claims. State medical boards modify advertising rules. A compliance tool that uses a fixed ruleset from six months ago is already dangerously outdated.
RegenCompliance solves this with automated daily monitoring. Every morning, our system checks FDA.gov for new warning letters, FTC.gov for new enforcement actions and press releases, and state medical board websites for updated advertising guidance. When a new enforcement action is relevant to healthcare marketing, we extract the specific language violations and add them to the compliance database within 24 hours.
This means the language that got a clinic in Florida a warning letter on Monday is already in your scanner's ruleset by Tuesday. You do not have to track enforcement actions yourself. You do not have to wait for your attorney to email you about new developments. The system handles it automatically, and every scan you run always uses the most current compliance data available.
See the full enforcement-alerts breakdownDOCUMENTATION
Every scan you run is permanently logged in your account with a full audit trail. This includes the original content scanned, the compliance score, every violation flagged, every rewrite generated, and the timestamp. This is not just a feature - it is your evidence that you took compliance seriously.
If the FDA or FTC ever contacts your clinic about marketing content, the first thing your attorney will ask for is documentation showing that you had a compliance review process. RegenCompliance provides that documentation automatically. Every scan generates a compliance report that can be exported as a PDF for legal review or as a CSV for internal record-keeping.
The audit trail also tracks your compliance score over time, giving you a clear picture of whether your marketing content is improving or degrading. This is valuable for clinic owners who delegate marketing to staff or agencies - you can verify that content is being checked before it goes live, and you can identify patterns in the types of violations your team tends to make.
See the full audit-trail breakdownPDF Export
CSV Export
Score Trends
Marketing Manager
Scans all website copy, ad creative, and social media posts before they go live. Uses the compliance library as a reference when briefing freelance writers.
Content Writer
Runs every blog post and email campaign through the scanner during the drafting process. Learns compliance patterns over time through the rewriter explanations.
Clinic Owner
Reviews audit trail to verify all marketing content was scanned before publishing. Monitors compliance score trends across the practice.
COLLABORATION
Compliance is not a one-person job. Your clinic owner, marketing manager, and content writer all touch marketing content at different stages. RegenCompliance includes three team seats with every subscription so the people who create, review, and approve content all have direct access to the scanner and compliance library.
Each team member gets their own login with full access to the compliance scanner, AI rewriter, and compliance library. All scan history is shared across the account, so the clinic owner can see what content has been scanned by the marketing team without asking for reports. This creates accountability and ensures that compliance scanning is part of your content workflow, not an afterthought.
Team seats eliminate the bottleneck of having a single person responsible for compliance checks. When your content writer can scan their own drafts before submitting them for review, violations get caught earlier in the process. When your front desk staff can check their patient communication templates, you reduce risk at every touchpoint. Compliance becomes embedded in your operations rather than bolted on at the end.
Under the hood
Every scan runs through a five-stage pipeline. Nothing about this is magic - it’s deterministic pattern matching layered with contextual AI analysis, all backed by a ruleset sourced directly from enforcement actions.
Your input (text / URL / file) is cleaned, de-duplicated, and split into analyzable units - sentences for paste mode, DOM elements for URL mode, text blocks for files.
Each unit is checked against 300+ phrase-level rules from FDA warning letters, FTC press releases, state medical board guidance, and DOJ healthcare fraud filings. Rule matches are surfaced with severity and source citation.
An Anthropic Claude model runs over flagged content to catch claims that rule-matching alone can't - implied disease claims, structure/function line-crossings, and testimonial-embedded violations. No-training setting enabled on every request.
Violations are classified as High / Medium / Low risk based on the original enforcement source and contextual severity. A 0-100 compliance score rolls up all flags, weighted by risk level and content length.
If you ask for a rewrite, Claude Sonnet regenerates the content under a compliance-aware prompt tuned on compliant healthcare-marketing examples. Your voice is preserved, violations removed, individual-variation disclosures added where appropriate.
Privacy
Your content is processed, scored, and stored only in your account. Nothing feeds into model training - Anthropic’s no-training flag is set on every request. Scans run over TLS and are encrypted at rest with AES-256.
Freshness
The ruleset updates daily from automated monitoring of FDA.gov, FTC.gov, and state medical board sites. New enforcement actions land in your scanner within 24 hours - no manual update cycle, no quarterly rule refresh.
Honest limits
This is an educational compliance tool. It is not a law firm, and it does not replace qualified healthcare marketing counsel. What it does is catch the pattern-matchable violations cheaply so your attorney’s time is spent on judgment calls.
GET STARTED
Every feature, every rule, every rewrite is designed specifically for healthcare marketing compliance - regenerative medicine, med spas, dental, plastic surgery, dermatology, weight loss, and more. No generic tools. No guesswork.