# Raycaster

> AI-native workspace for biopharma that keeps protocols, reports, and regulatory documents in sync with evolving science and guidance.

Raycaster is an AI-native workspace designed specifically for biopharma and life sciences teams working on regulatory submissions. It functions as a regulatory intelligence layer that sits on top of existing RIM and DMS systems, understanding how every rule, specification, and paragraph connects across your document ecosystem. The platform helps teams file stronger submissions with less rework by keeping protocols, reports, Module 2/3 sections, and quality documents synchronized as science evolves.

- **Regulatory Research** allows users to ask regulatory questions in plain language and receive cited answers pulled from FDA, EMA, ICH guidance, and internal standards, eliminating manual PDF hunting and cross-referencing.

- **Intelligent Drafting** generates protocols, amendments, investigator brochures, CSRs, narratives, control strategies, validation reports, and key Module 2/3 sections from your templates and data, letting writers review and refine rather than start from scratch.

- **Change Impact Analysis** traces the impact of any change across your entire dossier when you adjust an endpoint, limit, or process parameter, proposing aligned updates to keep all documents in sync.

- **Cross-Document Consistency** maintains alignment between protocols, CSRs, summaries, specs, methods, and Module 3 content with change-aware tracking built in.

- **Source Grounding** ties every suggestion back to guidance documents, prior submissions, or data with clear citations to exact paragraphs.

- **System-Agnostic Integration** works across Vault, Word, Excel, and existing document management stacks without requiring system replacement.

To get started, teams can book a demo through the platform to see how Raycaster maps document connections and manages change propagation. The platform serves clinical and medical writing teams, CMC and technical operations, nonclinical and toxicology groups, quality and compliance departments, and global regulatory teams coordinating submissions across regions.

## Features
- Regulatory research with cited answers from FDA, EMA, ICH guidance
- Auto-drafting of protocols, CSRs, and Module 2/3 sections
- Change impact analysis across entire dossier
- Cross-document consistency tracking
- Source grounding with citations to exact paragraphs
- Template-based document generation
- Regional requirement tracking
- Gap analysis for regulatory submissions
- Redline generation for document updates
- Integration with existing RIM and DMS systems

## Integrations
Vault, Microsoft Word, Microsoft Excel

## Platforms
LINUX, WEB

## Pricing
Paid

## Links
- Website: https://www.raycaster.ai
- EveryDev.ai: https://www.everydev.ai/tools/raycaster