Send Regulatory a cleaner first draft, every time.
Catch non-compliant claims in your medical device copy before Regulatory does - and before they cost you another launch delay.
Fewer rewrites. Faster approvals. Campaigns that ship on time.
Paste copy. Get flags. Fix faster.
Introducing our next-generation surgical platform - engineered to support clinicians across routine and complex procedures. Built with leading practitioners, our device is the safest on the market and can reduce complications by 80% in routine cases. It integrates seamlessly into existing theatre setups and supports the protocols teams already rely on.
It is trusted by leading hospitals worldwide and delivers best-in-class results. Patients recover faster than with traditional methods, with shorter recovery windows reported across early adopter sites, and the system eliminates the risk of infection thanks to its fully enclosed, single-use fluid pathway.
The platform's onboard analytics give teams a clear view of utilisation, case mix, and turnaround times. It is clinically proven to improve outcomes in every setting, from large teaching hospitals to community surgical hubs. The unit ships with structured training materials and ongoing access to our clinical education team.
From draft to ready-to-submit in five steps.
Drop in copy or a Word document. We handle the rest.
Sentence-by-sentence scan against common claim-risk patterns.
See exactly what may need evidence, softening or rewording.
Pick a lower-risk alternative, mark evidence held, or keep your wording.
Export a tighter draft so Regulatory's first read is closer to the last.
Cut review rounds, not standards.
Regulatory still reviews everything. You just send them a tighter first draft.
- Marketing Manager captures the features, benefits and product story
- Marcomms shape it into clear, compelling, customer-focused copy
- Design pulls it together on brand and ready to share
- Regulatory and Legal redline it, claims need evidence and rewording
- Back to Marcomms for changes, then re-check with Marketing
- Design update the document, then back to Regulatory and Legal
- Round and round, sometimes eight loops on a single piece
- Deadlines slip, tensions rise, backlogs grow across every team
- Marketing and Marcomms self-check claims as they draft
- Non-compliant issues flagged and fixed before anyone hits send
- Marcomms work with Design once to update the document, not round after round
- Regulatory and Legal get a near-final draft, not a first pass
- They focus on the complex calls, not the non-compliant fixes
- One round of amendments instead of six, seven, eight
- Every team stays calm, queues stay manageable
- Launch dates hold, budgets hold, working relationships hold
Where Claim Reviewr fits in
Marketing and Marcomms run a quick pre-check before handing over.
Regulatory still has the final say, they just get a tighter draft.
They pull it all together and make it look great and on brand.
They know the product inside out. They capture the features, the benefits, and why it's a great product.
They build on the initial content and shape it into something clear, compelling, and customer-focused.
They make sure every claim is accurate and backed by evidence.
Pre-check their copy before handing to Marcomms.
Check the copy for non-compliant content and claims.
They know the product inside out. They capture the features, the benefits, and why it's a great product.
Pre-check their copy before handing to Marcomms.
They build on the initial content and shape it into something clear, compelling, and customer-focused.
Check the copy for non-compliant content and claims.
They make sure every claim is accurate and backed by evidence.
They pull it all together and make it look great and on brand.
A quick Claim Reviewr pass between each handover means fewer surprises downstream, fewer loops, and fewer late-night rebuilds for Design.
Built specifically for medical device companies.
Claim Reviewr is grounded in medical-device advertising guidance - FDA 21 CFR 801/807 and FTC, MHRA Blue Guide and ASA CAP, EU MDR Article 7 / IVDR, and Health Canada Medical Devices Regulations. It flags wording that may mislead, overstate evidence, imply unapproved indications, exaggerate safety or performance, or require stronger substantiation.
Rules in. Checks out. Continuously.
Made for medical device teams. Not for pharma.
- In-house Marketing & Marcomms teams at medical device manufacturers
- Class I, II and III devices, plus IVDs
- Agencies writing copy on behalf of medtech clients
- Teams launching across US, UK, EU and Canada
- Pharmaceutical promotional copy (ABPI, PhRMA, EFPIA codes)
- Cosmetics, supplements or general wellness brands
- Veterinary medicines or animal health products
- Any use case outside medical-device advertising
Confidential, by default.
Workspace-isolated data with row-level security. Uploaded documents are stored privately, AI processing happens server-side, and your content is never used to train models.
Claim Reviewr is a pre-review tool for medical device marketing copy only. It does not replace your company's formal Regulatory, Medical or Legal approval, and is not intended for pharmaceutical promotional material. All content must still be reviewed and signed off by the appropriate internal teams before external use.
Ready to cut review rounds?
Send Regulatory a tighter first draft. Run your first check in minutes.