Evidra

Accelerate clinical and regulatory writing with evidence-linked AI drafting and automated compliance checks.

Intelligent Content Automation for Life Sciences

Pharmaceutical documentation is slow, expensive, and high-stakes. Writers start from blank pages while evidence sits fragmented across clinical trial databases, statistical outputs, SOPs, and historical submissions. Evidra converts that fragmented evidence into compliant first drafts, faster and with full auditable traceability.

Key Features

AI Draft Generation

Generates structured, evidence-aware drafts of regulatory documents (CSRs, protocols, safety narratives) aligned to industry guidelines.

Evidence-Linked Retrieval

Maintains strict bidirectional links between generated statements and clinical databases, so every claim is auditable.

Compliance Verification

Checks drafts automatically for missing sections, terminology drift, template deviations, formatting, and citation gaps.

Literature Synthesis

Summarizes and synthesizes medical publications, literature databases, and prior studies to build structured arguments.

Structured Reviews

Coordinates section ownership, comments, version control, and approvals among clinical, safety, and statistics teams.

Life Sciences Native

Built specifically for GxP, security, and evidence-traceable documentation requirements from the ground up.

Benefits & Use Cases

✓ Draft CSRs and Protocols 3x Faster
✓ Complete Audit Trail & Verification
✓ Automatic Compliance Validation
✓ Consolidated Multi-Stakeholder Review
✓ Accelerated Global Submission Pipelines
✓ Reduced Medical Writing Bottlenecks

Ready to streamline regulatory content?

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See It In Action

Real-world results and practical business scenarios demonstrating how our solutions deliver measurable outcomes.