Rematiq
Book a demo
For Pharma companies

Built for medicinal products that move the world.

Pharma development runs through thousands of controlled decisions, processes, and approvals. REMATIQ gives AI the structure to operate inside GxP environments, automating the work, preserving the proof, and keeping even the largest organizations in control.

The frameworks you live in

Pharma is rigorous. Its AI should be too.

  • REMATIQ combines industry-specific workflows, high-accuracy AI, and a complete GxP compliance framework, so teams can deploy AI rapidly, safely, and at enterprise scale.
  • 01

    Release Medicine Faster. Stay compliant easier. Remove the documentation burden across your product lifecycle with unmatched accuracy and repeatability.

  • 02

    Leaner operations. Free up hundreds of experts trapped in complex, redundant processes manually filling out template over template.

  • 03

    Audit-Ready AI. Pass any inspection with AI-systems optimised for control, repeatability, change management and all other systems the toughest pharma regulators require.

  • 04

    Handling complexity at scale. The only AI system handle the 10’000s of internal documents and external guidances contained in global QMS and R&D systems in pharma.

Use Cases

Mission-critical AI for the world’s most innovative companies.

Enable your brightest minds to focus on saving human life, while agentic workflows handle compliance and documentation burden.
Regulatory Intelligence

Regulatory Intelligence.

AI identifies all applicable regulatory requirements and checks your documentation for gaps in real-time.
Document Generation

Document Generation.

Execution agents generate any required document according to your guidelines in seconds.
Compliance Check

Compliance Check.

Create any document with a click of a button. Compliant with all requirements. Following your internal guides.
Submission Generation

Submission Generation.

Create any document with a click of a button. Compliant with all requirements. Following your internal guides.
Traceability Graph

Traceability Graph.

Create any document with a click of a button. Compliant with all requirements. Following your internal guides.
Already in production

R&D teams aren't evaluating Rematiq. They're running on it.

The efficiency gains aren't projections from a deck. They're what R&D leaders at Philips, Bayer and B. Braun are reporting back from production deployments.
R&D

Ship products. Not paperwork.

REMATIQ automates documentation, ensures compliance and ensures R&D projects stay on time.

Learn more
Regulatory Affairs

Defensible by default.

From regulatory intelligence to design control and submissions, REMATIQ automates the work that proves a product is ready. Keep timelines, demonstrate compliance, pass every audit.

Learn more
Quality Management

Audit-ready. Always.

Quality teams keep documentation continuously compliant, so inspections and audits no longer trigger weeks of scramble before every review.

Learn more
The pharma lifecycle, on REMATIQ

More output. More control. Faster cycles.

REMATIQ runs agentic workflows across the systems you already use, freeing experts from manual compliance work, raising the standard of documentation, and unlocking innovation capacity across every function.

Talk to an AI specialist.

Kim Bergstrand

Head of Sales

Book a 30 min call

  1. 01

    Identify use cases. REMATIQ impacts teams from clinical trials to TechOps and PSPV in simplifying and accelerating operations.

  2. 02

    Deploy agentic workflows. Our flexible platform handles any underlying data asset and automates the key workflow holding you back.

  3. 03

    Increase compliance. Every regulatory requirement is linked to the right process and automatically checked for compliance.

  4. 04

    Reduce cycle times. All processes accelerated, experts freed up to do their best work.

If your team spends more time formatting than building, we should talk.

Book a demo