For life sciences companies and their suppliers

Approved isn't the same as published.

Review approves your content before it goes out. We check what is actually live, on your site, your PDFs, your translations, and your distributors' listings, against what was approved, and keep the evidence of every fix.

Northwind NW-400 reagent kit3 findings
WherePublishedApproved
Spec sheet PDFDriftShelf life3 yearsShelf life2 years
Sales brochureDriftUse within, once opened60 daysUse within, once opened30 days
Campaign pageDriftIntended useDiagnostic testIntended useResearch use only

Illustration1

The problem

The wrong sentence looks exactly like a right one.

Each of these reads fluently, and each contradicts what the company approved. Your customer's quality team, a regulator, and an AI assistant all read it the same way.

Spec sheet PDF · Shelf life
Published3 years
Approved2 years

A customer who trusts the spec sheet may use a kit a year past the date on its label.

Sales brochure · Use within, once opened
Published60 days
Approved30 days

The document a lab was handed promises twice the working life the instructions allow.

Campaign page · Intended use
PublishedDiagnostic test
ApprovedResearch use only

One landing page makes a claim the company is not cleared to make, in words nobody flagged.

Illustration1

Why now

Regulators and customers are reading more closely.

Drug and biotech companies
200+
FDA enforcement letters on prescription drug advertising and promotion in 2025
Source: King & Spalding, 2025 Year in Review: FDA Drug and Device Advertising and Promotion Enforcement, January 2026.

Of the letters sent to drug and biologic makers, all but five came after the FDA's announcement in September 2025. They cite TV ads, web pages, social posts, and printed materials, and every one is public.

Suppliers to life sciences
Your specsare your customers' inputs

Your customers make manufacturing and quality decisions from what you publish. When a shelf life, material, or sterilization statement disagrees with your validated data, it becomes their deviation, their audit question, and your harder conversation.

How it works

We start where your review ends.

After review, copies multiply: older PDFs stay online, translations lag behind, and a distributor keeps last year's spec. We work alongside the review you already run.

Before publishing · your team

You approve the content.

Medical, legal, regulatory, and quality review decide what may be said, and set the approved specs, claims, and intended use.

After publishing · Blue Prospect

We check what's live, everywhere.

Every page, PDF, translation, and partner listing is read against what you approved. Anything that contradicts it, or claims more than it supports, becomes a finding.

What we check

Everything you publish, against what you approved.

  1. 01

    Specs

    Shelf life, storage, materials, dimensions, standards met, and compatibility, wherever a product is described.

  2. 02

    Claims and intended use

    What a product is cleared or approved for, and any claim your approved source does not support.

  3. 03

    Risk, storage, and handling

    Safety information, warnings, and handling instructions that must appear, and must match.

  4. 04

    Translations

    Every market says the same approved thing, including after the English changes.

  5. 05

    PDFs and collateral

    Spec sheets, brochures, sales decks, and the older files still linked from somewhere.

  6. 06

    Partner and distributor listings

    The pages other companies publish about your products. When one is wrong, we tell you what to ask them to change.

The evidence

Every finding comes with its evidence.

Nothing in a finding is our opinion: it quotes your own page against your own approved source. Whoever fixes it, your team or us, the fix is verified and kept in your portal.

We don't decide what is compliant. Your regulatory and quality teams do. We make sure what you publish matches their decisions.

When they change a decision, the change reaches every surface, not just the one someone remembered.

Your teams decide
NW-400 · Shelf life2 yearsApproved by Quality
We make sure it matches
  • Product page2 yearsMatches
  • Spec sheet PDF2 yearsMatches
  • Sales brochure2 yearsMatches
  • German product page2 yearsMatches
  • Distributor listing2 yearsMatches
  • Sales deck2 yearsMatches
Questions

What people ask first

Do you make us compliant?

No. Your regulatory and quality teams decide what is approved and what is compliant. We make sure what you publish matches their decisions, and we keep the evidence.

Does this replace our review process?

No. Your review approves content before it goes out. We check what is actually published afterward, everywhere it appears, and again whenever anything changes.

Which content do you check?

Your website and landing pages, your PDFs and other collateral, your sales materials, your translations, and the listings your partners and distributors publish about your products.

What happens when a distributor's page is wrong?

We show you the page, the sentence, and the approved spec it contradicts, and draft the correction for you to send. Only the distributor can change its own page, so the finding stays open until it matches.

Do you work in other languages?

Yes. Every market is checked against the same approved source, so a change in English is followed into each translation.

How you start

See your own findings first.

A first read of a few of your pages is free, and it comes before you commit to anything.

How it starts
  1. 01A first read

    A few of your pages, free. No source needed, nothing to connect.

  2. 02Findings

    Your portal opens, with findings on everything you publish from day one.

  3. 03Your source

    Your approved specs, claims, and labeling, defined with you.

  4. 04Watch or Run

    Fix from the findings yourself, or let us carry every change everywhere.