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From the first draft of a CSR to the next call on an HCP, life sciences runs on decisions that are slow, manual and scattered. Each solution below takes one of them and returns an answer your team can act on: sourced, explained and owned.

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Technology · Solutions

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  1. 01Regulatory IntelligenceWhich rule change affects our products, and by when?Regulatory affairs
  2. 02Medical Writing AutomationSubmission-ready drafts in hours, not weeks.Medical writing and clinical teams
  3. 03NUDGE OmnichannelThe next best action for every HCP.Brand and commercial teams
  4. 04MLR AutomationContent that passes review first time.Promotional and medical content teams, MLR reviewers
  5. 05Market Research ToolA sourced go or no-go on a new market, in minutes.Strategy, business development and market access
  6. 06HTML Deliverable QCHCP emails that render right in every inbox.Digital and content operations
  7. 07IQ HubPapers from first draft to journal submission.Medical affairs and publications teams

Where life sciences slows down, and how we speed it up.

01Regulatory Intelligence

Know which regulatory change matters, before the deadline does.

AI-powered regulatory intelligence that tracks global rule changes and tells you what they mean for your products.

Who it's for: Regulatory affairs teams

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The problem

  • Updates from dozens of agencies, in different formats and languages
  • The one change that matters gets lost in the noise
  • Impact assessments are slow and manual

The value we bring

  • One live view of regulatory change across your markets
  • Only the updates relevant to your portfolio, in plain language
  • Clear impact on labels, submissions and materials, before deadlines
See how Regulatory Intelligence works

How it works

  1. 1TrackMonitors updates from health authorities across your markets, in every format and language.
  2. 2FilterMatches each update to your portfolio, so you see only what applies to your products.
  3. 3ExplainSummarises each relevant change in plain language.
  4. 4AssessShows the impact on labels, submissions and materials, with the deadline attached.
In
Regulatory updates and guidance from agencies across your markets, plus your product portfolio.
Out
A live change feed, plain-language summaries, and an impact view per product with deadlines.
Who uses it
Regulatory affairs, labelling and regulatory operations teams.

02Medical Writing Automation

Regulatory documents, drafted in hours. Every sentence cited.

An AI medical writing studio inside Microsoft Word that drafts only from your sources. No source, no sentence.

Who it's for: Medical writing and clinical development teams

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The problem

  • CSRs, safety reports and CERs take weeks of expert time
  • Every day a submission slips delays patients and revenue
  • Generic AI hallucinates and cannot be audited

The value we bring

  • First drafts of CSRs, protocols, PSURs and CERs in hours
  • Sentence-level citations and code-checked numbers
  • Works in Word with your templates, with a full audit trail
See how Medical Writing Automation works

How it works

  1. 1Connect your sourcesStudy data, upstream documents, templates and prior submissions.
  2. 2Plan the documentStructure, sources and evidence are mapped before a word is drafted.
  3. 3Draft in WordEvery sentence is written from, and cited to, a source. No source, no sentence.
  4. 4Check the numbersFigures are code-checked against the underlying data.
  5. 5Review and sign offYour writers edit in Word, on your templates, with a full audit trail.
In
SDTM/ADaM datasets and TLFs; protocol, SAP and investigator brochure; legacy files (scanned PDF, RTF, Word, Excel); your templates and standards.
Out
First drafts of CSRs, protocols, PSURs and CERs.
Who uses it
Medical writers, reviewers, biostatisticians, regulatory strategists and QC.

03NUDGE Omnichannel

From brand plan to the next best action, for every HCP.

One engine that builds the brand plan from market evidence and turns it into explained weekly actions for every healthcare professional.

Who it's for: Brand, marketing and commercial excellence teams

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The problem

  • Fewer reps, more channels: every visit has to count
  • Brand plans and field actions drift apart in separate systems
  • Little proof of what omnichannel spend returns

The value we bring

  • A living brand plan that updates as the market moves
  • One explained next best action per HCP each week, pushed to your CRM
  • Clear ROI per channel, with compliance built in
See how NUDGE Omnichannel works

How it works

  1. 1Read the marketTakes in market evidence for your brand and therapy area.
  2. 2Build the brand planTurns that evidence into a living plan that updates as the market moves.
  3. 3Set the week's actionsGives one next best action per HCP each week, with the reason behind it.
  4. 4Push to the fieldSends those actions into your CRM, where reps already work.
  5. 5Measure and adjustTracks return per channel and feeds results back into the plan.
What it brings together
Brand strategy, channel mix, field action and results, in one engine instead of separate systems.
Who uses it
Brand managers, marketing and commercial excellence teams, and field leadership.

04MLR Automation

Get content right first time through MLR review.

One AI-assisted platform to create, check and approve promotional and medical content, working on top of Veeva Vault.

Who it's for: Promotional and medical content teams, and MLR reviewers

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The problem

  • A promotional job takes about 15 days on average (Vodori, 2025)
  • Most content fails its first Medical, Legal or Regulatory round
  • Claims and references are checked again and again by hand

The value we bring

  • AI compliance, claim and code checks before submission
  • Content built from pre-approved claims and modules
  • Fewer review rounds, with e-signatures and a full audit trail
See how MLR Automation works

How it works

  1. 1CreateBuild content from pre-approved claims and modules, not from a blank page.
  2. 2CheckAI runs compliance, claim, reference and code checks before anything goes to review.
  3. 3ReviewContent reaches Medical, Legal and Regulatory reviewers cleaner, so fewer rounds are needed.
  4. 4ApproveSign off with e-signatures, with every change and decision kept in a full audit trail.
What it handles
Promotional and medical content, working on top of Veeva Vault.
Who uses it
Content creators, brand and medical teams, and MLR reviewers.

05Market Research Tool

Market-entry decisions in minutes, not months.

Ask a market question in plain language and get a sourced Go or Watch recommendation, with a full downloadable dossier.

Who it's for: Strategy, business development and market access teams

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The problem

  • Market studies take weeks and cost heavily
  • Regulatory, commercial and competitive evidence is scattered
  • Reports go stale the day they land

The value we bring

  • A clear Go, Watch or Do not enter recommendation with a weighted scorecard
  • Every score linked to its source, date and confidence
  • Ongoing monitoring that flags when a market changes
See how Market Research Tool works

How it works

  1. 1AskType a market-entry question in plain language.
  2. 2GatherThe tool pulls regulatory, commercial and competitive evidence for that market.
  3. 3ScoreEach factor is rated on a weighted scorecard, with its source, date and confidence.
  4. 4RecommendYou get a Go, Watch or Do not enter call and a full downloadable dossier.
  5. 5MonitorThe market keeps being watched, and you are alerted when something changes.
In
Regulatory requirements and filing pathways; epidemiology and addressable population; pricing, reimbursement and HTA precedent; competitor footprint, channels and access dynamics.
Out
The recommendation and scorecard, plus regulatory strategy, market potential, entry strategy, pricing corridor and launch sequence in the dossier.
Who uses it
Strategy and business development, regulatory strategists, market access leads, region heads and country GMs.

06HTML Deliverable QC

Every HCP email, perfect in every inbox.

Check how your emails render across 17 email clients, with automated code checks and a client-ready QC report.

Who it's for: Digital, content operations and email production teams

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The problem

  • An approved email can still break in Outlook, Gmail or dark mode
  • Manual test sends and screenshots for every deliverable
  • Accessibility and link issues are easy to miss by eye

The value we bring

  • One QC run across desktop, webmail and mobile clients
  • Automated accessibility, dark mode, link and deliverability checks
  • A clear pass, warn or fail QC report for every email
See how HTML Deliverable QC works

How it works

  1. 1Submit the emailAdd the HTML for an approved HCP email.
  2. 2Render everywhereSee it across 17 email clients: desktop (e.g. Outlook), webmail (e.g. Gmail, Yahoo) and mobile.
  3. 3Run the checksAutomated accessibility, dark mode, link and deliverability checks.
  4. 4Share the reportGet a pass, warn or fail QC report you can hand straight to the client.
What it covers
HTML emails only.
Who uses it
Email developers, digital producers, QC teams and account teams.

07IQ Hub

Every publication, from first draft to journal submission.

One platform where medical teams plan, check, review and submit scientific papers together.

Who it's for: Medical affairs and publications teams

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The problem

  • Manuscripts, versions and feedback scattered across inboxes
  • Errors found late, at review or after submission
  • Journal selection and submission documents take time

The value we bring

  • Manuscript quality checks with STROBE, CONSORT, CARE and SPIRIT
  • Built-in MLR review with version compare and audit trail
  • Journal match and ready-made submission documents, in English and Japanese
See how IQ Hub works

How it works

  1. 1PlanSet up the publication and bring the team, manuscript and timeline into one place.
  2. 2CheckRun manuscript quality checks against the right reporting guideline.
  3. 3ReviewUse built-in MLR review, with version compare and a full audit trail.
  4. 4SubmitGet a journal match and ready-made submission documents, in English and Japanese.
Reporting guidelines covered
STROBE (observational studies), CONSORT (randomised trials), CARE (case reports) and SPIRIT (trial protocols).
Who uses it
Medical affairs and publications teams, medical writers, authors and reviewers.

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