Rematiq
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For Quality Management

Audit-ready. Always.

REMATIQ creates continuous traceability across your compliance work, connecting every requirement to the processes, work instructions, templates, and evidence that prove it. No gaps. No scrambling. Always ready.

Value

Every requirement covered. Every gap closed.

When regulations move, your compliance moves with them. REMATIQ uses AI to detect change, understand impact, and keep every process, document, and requirement synched.

Your week, today

  • Manual document work wherever you look. Thousands of SOPs and work instructions, every change takes dozens of hours.

  • Complexity killing productivity. Well-intended iterations over years create an interlinked web of detailed instructions slowing down teams.

  • Work equals filling out templates. Some of the world’s smartest peoples spend their days filling out excel files.

  • Audit prep is a fire drill. The auditor shows up, half the team stops for two weeks to brush up documentation.

Your week on Rematiq

  • Smart and compliant automation. All work in your QMS linked and traced, reliable AI agents simplify and automate process work.

  • Clear processes, simplified. Redundancies, duplicates, complications - all removed with smart agents.

  • Work equals checking agents work. Agents fill out templates, humans check and ensure quality.

  • Audit-ready, every day. Compliance isn't manufactured before an audit. It's a continuous loop ensured by the system.

Use Cases

Built for what cannot fail.

Automate complex, multi-step quality management workflows across teams, systems, and stakeholders, while keeping every action traceable, reviewable, and compliant.
Document Generation

Document Generation.

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

Compliance Check.

Ensure compliance of any deliverable in your QMS against global applicable requirements.
Traceability Graph

Traceability Graph.

Automatically link extracted data objects of any regulation, process, test or product documentation to easily facilitate change management and migrations.
Already in production

QM teams aren’t evaluating Rematiq. They’re running on it.

Real impact measured in large-scale deployments at the world’s most innovative companies.
MedTech

Continouos compliance loops

QMS documents turned in to data, each step in every work instruction linked to the corresponding regulatory requirement and automatically updated for every process or regulation change.

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Pharma

14 weeks - 7 weeks

Global PSPV, Clinical Trials and Manufacturing teams accelerate regulatory impact assessments by weeks while experiencing 75% efficiency gains.

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Where REMATIQ sits in your QM workflow

From process setup to agentic execution.

REMATIQ doesn’t replace your eQMS. It runs on top of it, automating workflows, completing templates, and keeping every step compliant, traceable, and ready to review.

Talk to an AI specialist.

Kim Bergstrand

Head of Sales

Book a 30 min call

  1. 01

    Process compliance. Identify all global applicable regulatory requirements, find gaps and adapt your processes to remain compliant.

  2. 02

    QMS Streamlining. Identify redundancies, duplicates, gaps between local and global and more with agentic workflows.

  3. 03

    Audits, automated. Automate internal audits through agentic reviews. Be ready for any health authority agent running your audits.

  4. 04

    Execution agents. Run GxP-compliant agents to fill out any templates in your QMS according to the SOPs and guidances you set.

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

Book a demo