Heads of Market Access
& Value
Looking to reduce budget spend and accelerate time-to-market.
Our streamlined process takes you from raw data to a submission-ready dossier in five strategic steps.
Securely upload your clinical data, studies, and source materials.

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

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

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

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

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.
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.
❌ 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.
✅ 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.
In time-to-first-draft for Module 4 tables
In data transfer, minimizing QC cycles
Internal review times with built-in QC and source-linking
Export directly into the perfectly formatted, official G-BA Word template
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.
Our agentic workflow manages the entire creation process, from initial data to a fully structured document, dramatically reducing manual effort.

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

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.


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.
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.



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


Seamless Refinement and Submission
From first draft to final export, the entire process is designed for efficiency and ease. Refine content, provide feedback, and export a perfect, submission-ready document in minutes.

Easy-to-Use Content Editing Workflow
Making changes is simple. Review and modify any AI-generated text with a seamless and intuitive content editing workflow that feels natural and efficient.

Copilot Control for Human Feedback
Your expertise makes the AI smarter. Use the Copilot control to provide direct human feedback to the agentic workflow, refining the output for this project and improving the AI for the next one.

Export Dossiers in a Strict Regulatory Word Format
Forget about tedious reformatting. Export your final dossier into a Word document that strictly adheres to regulatory formatting and styling requirements, ready for immediate submission.

Generate Dossiers in Your Local Language
Work without language barriers. Effortlessly generate high-quality, accurate dossiers in your local language, improving clarity and efficiency for global teams.
This platform provides a strategic advantage for: