An AI-native platform to
authoring reimbursement
dossiers

Leverage our advanced Agentic workflows to create compliant, submission-ready benefit assessment dossiers faster than ever. You direct the narrative; our AI handles the rest.

Authoring Workflow

Our streamlined process takes you from raw data to a submission-ready dossier in five strategic steps.

01
Upload Data

Securely upload your clinical data, studies, and source materials.

02
Define Strategy

Input your key narrative and strategic goals to steer the AI narration.

03
AI Authoring

Our agents generate the first draft, guided by your strategic inputs.

04
Review & Refine

Use the Copilot and editor to guide, edit, and approve the content.

05
Export

Download your dossier in a strict regulatory format, ready for submission.

Our AI agents have proven expertise to author
GVD
AMNOG

Germany: G-BA (AMNOG) Dossier

We bring efficiency to authoring key strategic sections, enabling you to build a powerful narrative around your product's clinical and economic value.

Clinical Value Messaging

Strategic Storytelling: You're in the driver's seat. Effortlessly generate the crucial results section (Module 4, Section 4.3.2.3.1) by strategically selecting endpoints and authoring your pivotal RCT studies.

Evidence Integration:
Seamlessly integrate your source data. Craft compelling tables and narratives directly from Clinical Study Reports (CSRs), figures, and statistical outputs.


Economic Value Messaging

Foundation for Negotiation: A strong clinical value story is the essential foundation for successful price negotiations. By precisely articulating the 'Zusatznutzen' (additional benefit), you create the strongest possible position for demonstrating economic value.

Global Value Dossier (GVD)

The GVD is your product's core value story. Our platform provides the ultimate flexibility to build a comprehensive and persuasive GVD from the ground up.

Clinical Value Messaging

Total Narrative Control: You define the dossier's outline. Start with your core Global Value Proposition (GVP) and tailor the story to highlight your product's unique clinical advantages.

Unify Your Evidence: Consolidate your entire evidence base with ease. You can bring in any source—publications, Systematic Literature Reviews (SLRs), Indirect Treatment Comparisons (ITCs), and key data tables—to author robust and well-supported clinical sections.


Economic Value Messaging

Author with Impact: Translate your clinical data into a compelling economic argument. Provide targeted inputs to author sections that clearly demonstrate cost-effectiveness, budget impact, and the overall value your product brings to healthcare systems.

The AMNOG Blueprint: From Clinical Trial Statistical Data to Dossier Tables in 48 Hours.

The validated GenAI platform that automates AMNOG Module 4. We populate your G-BA template directly from clinical trial statistical data with >99% accuracy. The exact blueprint used to transform the AMNOG process for large Pharma portfolios.

Stop the Manual Grind. Embrace Intelligent Automation.

The Old Way: Months of Manual Effort

❌ Endless Data Mining

Manually searching hundreds of pages across multiple clinical trial statistical datasets, publications, and appendices for a single data point.

❌ High-Risk Data Transfer

Constant fear of copy-paste errors, incorrect decimal places, or missed footnotes leading to endless, expensive QC cycles.

❌ Massive Vendor & Resource Costs

The average AMNOG dossier costs €800,000, largely driven by the manual authoring and review of Module 4.

The New Way: The AMNOG Blueprint

✅ Intelligent Data Retrieval

Our AI reads, understands, and indexes all your source documents, finding the exact data you need in seconds.

✅ >99% Accurate Population

We automate the data transfer directly into the G-BA template, eliminating manual errors and validating data against the source.

✅ Significant Cost & Time Reduction

Slash vendor dependency and free up your internal experts to focus on strategy, not data entry. Generate drafts in days, not months.

The Tangible Impact of Automation

90%
REDUCTION

In time-to-first-draft for Module 4 tables

>99%
ACCURACY

In data transfer, minimizing QC cycles

50%
FASTER

Internal review times with built-in QC and source-linking

100%
COMPLIANT

Export directly into the perfectly formatted, official G-BA Word template


10+ reimbursement dossiers generated in AMNOG using our Agentic platform for around OBU and BBU areas

Agentic Foundation, Expert Direction

Stop wrestling with manual document creation and focus on what matters: your strategic narrative. Our platform automates the foundational work while keeping you firmly in control.Author End-to-End Dossiers Our agentic workflow manages the entire creation process, from initial data to a fully structured document, dramatically reducing manual effort.

Author End-to-End Dossiers

Our agentic workflow manages the entire creation process, from initial data to a fully structured document, dramatically reducing manual effort.

Generate to a Strict Template Outline

Ensure compliance from the start. The AI builds your dossier precisely according to your required template outline, guaranteeing structural integrity every time.

Align AI Output with Your Strategy

Translate your market access narrative strategy into action. Our easy-to-use, human-in-the-loop workflow allows you to guide the AI agents, ensuring the final content and tone perfectly match your expert direction.

Uncompromising Accuracy and Confidence

Submit your work with the highest degree of confidence. Our system is designed to ensure accuracy, transparency, and compliance are built into every section of your dossier.

Easy-to-Use Confidence Grading System

Instantly identify areas that need your expert eye. Our system flags sections with a clear, intuitive confidence score, so you know exactly where to focus your review.

Accurate Citations to the Sources

Eliminate referencing errors and ensure full traceability. The platform automatically generates precise and accurate citations, linking directly back to the source materials.

Built for the Leaders of Market Access

This platform provides a strategic advantage for:

Heads of Market Access
& Value

Looking to reduce budget spend and accelerate time-to-market.

G-BA Dossier Leads & Managers

Tasked with delivering high-quality submissions on time.

Medical Writing & Regulatory Affairs Teams

Responsible for the accuracy and
integrity of clinical data.

Your AI Analyst for Pharma Market Access
Simplifying complex regulatory workflows with speed, accuracy, and compliance.