EvidenceAi™ Suite

Super intelligence for every step of a
real-world evidence study

Guideline-grounded modules that take a study from concept to protocol, analysis plan, code, report and manuscript — each output feeding the next, with your expertise in the loop.

HARPER & EMA GVP Module VIII ICH E9(R1) estimand framework Human in the loop 50 free credits on sign-up
Start free — 50 credits included View pricing Request pilot access
OverviewModulesEvidenceSecurityPricingFAQ
Overview

First drafts in minutes, not weeks1,2

Results from the pilot evaluation with practising evidence professionals.

~99%calendar time saved per document (46.6 days on average)
~98%human effort saved per document (11.5 days on average)
7.85/10scientific quality (5.0 = equivalent to a human first draft)
9.2/10overall user satisfaction
To be presented at ISPOR Europe 2026 (Vienna, 8–11 November): 20 evaluations by 7 respondents from 7 organisations across 8 modules; mean scores on a 0–10 scale. Early-adopter sample; data collection ongoing. All outputs are first drafts for expert review. Full results and references →
The RWE study pipeline
Strategy
GuideAi™ Included
ExploreAi™
ConceptAi™
FeasibilityAi™
Development
ProtocolAi™
SAPAi™
CodeAi™
DataAi™ Soon
AnalyzeAi™ Soon
Dissemination
ReportAi™
ManuscriptAi™
AppraiseAi™
AssessAi™

11 modules available, 2 coming soon.

Modules

Every module, in detail

Use one module on its own or run the full pipeline. Credit costs are per successful run.

GuideAi™
Your RWE methodology compass
Included in all plans
What you get
Interactive guidelines directory with canonical references, methodology summaries, and regulatory guidance for any RWE question.
Ideal for: Any team starting a new study or looking for methodological orientation.
Try it free
ExploreAi™
Landscape intelligence in minutes
1 credits / run
What you get
Comprehensive data source inventory, literature gap analysis, competitor study mapping, and regulatory precedent review — structured as a 5–10 page landscape brief.
Ideal for: Evidence strategists, medical affairs teams, early-stage study planning.
Try it free
ConceptAi™
From idea to concept sheet in one run
5 credits / run
What you get
A 3–7 page HARPER-aligned study concept sheet covering objectives, PICOTS framework, study design rationale, preliminary data source selection, and regulatory context.
Ideal for: RWE scientists, pharmacoepidemiologists, regulatory affairs teams.
Try it free
FeasibilityAi™
Go/no-go before you commit a budget
15 credits / run
What you get
A 5–30 page feasibility report with patient count estimates, ICD code coverage analysis, database scoring against study parameters, risk evaluation, and a clear Go/No-Go recommendation — plus a database landscaping spreadsheet.
Ideal for: Study teams evaluating data sources, CRO partners, sponsors.
Try it free
ProtocolAi™
Publication-ready protocol in hours, not weeks
20 credits / run
What you get
A 40–70 page HARPER + EMA GVP VIII-compliant study protocol covering background, objectives, methodology, statistical considerations, ethical provisions, and two HARPER tables justifying every design choice.
Ideal for: Pharmacoepidemiologists, regulatory teams, ENCePP submissions.
Try it free
SAPAi™
Statistical rigour, ICH E9(R1) aligned
20 credits / run
What you get
A 30–50 page statistical analysis plan with estimand framework, sample size, analysis populations, exposure/outcome/confounder evaluation, subgroup and sensitivity analyses — plus 10–12 study-tailored TFL shells in Excel.
Ideal for: Biostatisticians, statistical programmers, regulatory submissions.
Try it free
CodeAi™
Analysis-ready code, aligned to your SAP
15 credits / run
What you get
A complete statistical code package in R, SAS, Python, or Stata — annotated, production-ready, aligned to your SAP and data model (OMOP, FHIR, claims). Delivered as a ZIP archive with macro libraries and execution scripts.
Ideal for: Statistical programmers, data scientists, OMOP/FHIR specialists.
Try it free
DataAi™
From raw data to analysis-ready dataset
Coming soon
What you get
Data preparation, cleaning, and structuring for RWE analysis across OMOP, FHIR, claims, EHR, and registry sources.
Ideal for: Data engineers, analysts, OMOP specialists.
AnalyzeAi™
Primary and sensitivity analyses, output-ready
Coming soon
What you get
Run primary and sensitivity analyses with output-ready tables, figures, and listings aligned to your SAP.
Ideal for: Biostatisticians, data analysts, study teams.
ReportAi™
Clinical study report in regulatory format
25 credits / run
What you get
A 100–200 page clinical study report structured per ICH E3, RECORD, or GVP Module VIII, integrating protocol, results tables, and narrative sections.
Ideal for: Regulatory affairs, medical writing teams, sponsor submissions.
Try it free
ManuscriptAi™
From report to publication-ready manuscript
10 credits / run
What you get
A polished first draft manuscript structured for your target journal and reporting guideline (STROBE, RECORD-PE, CONSORT, PRISMA), with inline citations and discussion section.
Ideal for: Medical writers, scientists, publication planning teams.
Try it free
AppraiseAi™
Expert critique in seconds
1 credits / run
What you get
A structured critical appraisal of any manuscript, protocol, SAP, or report — identifying methodological strengths, limitations, reporting gaps, and quality scores against CASP, STROBE, CONSORT, PRISMA, or GRADE frameworks.
Ideal for: Peer reviewers, quality teams, regulatory assessors.
Try it free
AssessAi™
Dossier acceptability before you submit
1 credits / run
What you get
A structured regulatory and HTA dossier acceptability report — probability of success, stakeholder context, major and minor comments, and a prioritised action plan — from the perspective of your selected body.
Ideal for: Regulatory affairs, HEOR directors, market access teams.
Try it free
Evidence

How the outputs were rated

Measured with the EvidenceAi™ Assessment Survey (EAS). Comparative domains use a 0–10 scale where 5.0 means equivalent to an experienced human first draft; absolute domains are rated on their own scale.

Comparative domains (5.0 = human first draft)

8.95
9.85
8.25
7.85
6.95

Absolute domains (0–10)

9.05
9.10
9.20
Vertical marker = 5.0, the human-equivalent first draft. Means of 20 evaluations.

Pilot at a glance

Practising evidence professionals from 7 organisations evaluated 8 modules (20 evaluations).

Read with care. Early-adopter sample with wide confidence intervals; error patterns were the weakest domain. Outputs are first drafts and always need expert scientific review.

Abstracts & full results

Security

Three levels of security, by design

Study documents are confidential. The EvidenceAi™ Suite protects them at the platform, at the data and at the intelligence layer — and lets your organisation decide which super intelligence does the work.

Level 1

A securely built platform

The protections you expect from a well-designed web application and API.

  • Encrypted connections (HTTPS) between you and the platform
  • Authenticated accounts with protected passwords and controlled access
  • Hardened forms and requests: input validation, request protection and parameterised database queries
  • Access keys and settings kept server-side, never exposed in the browser
  • Separate development, pilot and production environments
Level 2

We do not keep your documents

What is not stored cannot be compromised.

  • Source documents and prompts are processed in memory and not retained on our platform
  • Only what is needed to deliver and bill the service is kept
  • You keep the generated deliverables; we keep no copy of your confidential inputs
Level 3

Your super intelligence, your choice

Organisations work with the super intelligence they already trust.

  • Connect the provider and model approved by your organisation
  • Use an in-house super intelligence behind your own firewall with our tool
  • Your data stays within the boundaries your governance defines
Pricing

Simple, transparent pricing

Pay only for what you generate. Credits never expire. Start free — 50 credits are included with every new account, worth $4,249 at our most popular pack rate. Organisations can move to an Enterprise plan with no credit tracking.

Credits never expire

Credits remain valid as long as your account is active and at least one purchase or generation was made in the preceding 24 months. No monthly fee.

Protected generations

Credits are non-refundable, but credits used in a failed generation are automatically restored to your balance.

Re-generation guarantee

If a deliverable does not meet your expectations, contact us within 48 hours and we will regenerate it at no credit cost.

50
free on sign-up
$0
no card needed
Worth $4,249
Dashboard
5
credits
$499
$99.80 / credit
Get started
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10
credits
$949
$94.90 / credit
Save 5%
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20
credits
$1,799
$89.95 / credit
Save 10%
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most popular
50
credits
$4,249
$84.98 / credit
Save 15%
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100
credits
$7,999
$79.99 / credit
Save 20%
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Prices in USD; Stripe handles local currency conversion. See Terms of Use for the credit policy.
Named users run any module any number of times, subject only to concurrency limits — no credit tracking. Ideal for organisations with continuous evidence-generation needs. Access is granted automatically to any user registered with your organisation’s email domain.
Unlimited Starter
∞ Unlimited executions 5 concurrent jobs 10 workspaces 25 users 97.00% uptime SLA
Standard email support
Unlimited Business
∞ Unlimited executions 20 concurrent jobs 30 workspaces 75 users 98.00% uptime SLA
Priority support · API access
Unlimited Enterprise
∞ Unlimited executions 50 concurrent jobs ∞ workspaces ∞ users 99.95% uptime SLA
Dedicated CSM · SSO · Dedicated infrastructure
✓API access
✓Audit logs
✓Dedicated Customer Success Manager
✓Single Sign-On (SSO)
Request an Enterprise proposal
Access is intended for the client’s internal clinical research activities. Systematic reselling, benchmarking against competitors, or using the Platform to train external models is prohibited. Fair Use Policy applies — see Terms of Use.
Up to 50% off Enterprise pricing
The same Enterprise plan structure — named users, unlimited module executions within Fair Use, no credit tracking — extended to universities, hospitals, NGOs and public health institutions at a reduced rate.
Unlimited Starter
∞ Unlimited executions 5 concurrent jobs 10 workspaces 25 users 97.00% uptime SLA
Standard email support
Unlimited Business
∞ Unlimited executions 20 concurrent jobs 30 workspaces 75 users 98.00% uptime SLA
Priority support · API access
Unlimited Enterprise
∞ Unlimited executions 50 concurrent jobs ∞ workspaces ∞ users 99.95% uptime SLA
Dedicated CSM · SSO · Dedicated infrastructure
✓API access
✓Audit logs
✓Dedicated Customer Success Manager
✓Single Sign-On (SSO)
Apply for the reduced rate
Eligible organisations receive up to 50% off standard Enterprise pricing. Eligibility and final pricing are confirmed on application. Fair Use Policy applies — see Terms of Use.
Optional services

Template & branding customisation

Your house style, headers, footers and cover pages applied to every Word and Excel deliverable.

Contact us →

SOP & prompt customisation

Terminology, therapeutic-area emphasis and disclaimer language adjusted within existing modules.

Contact us →

Database & source registry filtering

FeasibilityAi™ and ExploreAi™ limited to the data sources your organisation is licensed to use.

Contact us →

Admin enablement & training

Console access for up to two named admins, a live training session, a quick-reference guide and follow-up support.

Contact us →

Your own AI provider

Run the Suite on your organisation’s own model agreement, or on an in-house model.

Contact us →

Scientific oversight & review

Our scientists review what the Suite generates — a turnkey service for protocols, SAPs and reports.

See Services →
FAQ

Frequently asked questions

Credits do not expire provided your account remains active and at least one purchase or generation was made in the preceding 24 months. A 90-day reactivation notice is sent before any credits are forfeited. See Terms of Use.
Credit purchases are non-refundable. Credits consumed in a failed or interrupted generation are restored automatically, and if an output does not meet your expectations you can contact us within 48 hours for a free re-generation.
One deduction occurs when a generation completes successfully and the output is available. Failed or interrupted generations do not consume credits.
Individual credits are tied to one account. Enterprise plans remove credit tracking: every named user can run modules under one organisational agreement, subject only to concurrency limits.
Documents are text-extracted in your browser, so the original file never leaves your device. Submitted text is processed in server memory and discarded, and by default is sent only to the model provider used to generate your output, under business terms that exclude training on your inputs. Organisations can use their own provider or an in-house model instead. See the Privacy Policy.
Enterprise plans are agreed directly and invoiced annually in euros. Named users run modules without credit tracking within Fair Use. Healthcare, academic and non-profit organisations receive up to 50% off. Pro-rata pricing applies to mid-year starts. Contact us for a proposal.
Yes. Our scientists provide oversight and review of AI-generated documents as a turnkey service. See Services.

Start your first study today

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