AI Assistants for GMP Professionals.

Responsible AI tools to support documentation, SOP drafting, deviation writing, risk assessments and quality system work in regulated cannabis environments.

The pharmaceutical industry is beginning to integrate AI tools responsibly into quality and manufacturing workflows. ECI is developing a set of structured AI assistants specifically for cannabis GMP professionals — designed to accelerate routine documentation tasks while maintaining the human review and accountability that GMP requires.

All ECI AI tools are designed within the EMA, ICH and EU GMP guidance on the use of AI in pharmaceutical manufacturing contexts.

Documentation

SOP Drafting Assistant

Structured prompts and templates for drafting GMP-compliant SOPs for cannabis manufacturing, cultivation and quality operations.

Opening Q3 2026
Quality Systems

Deviation & CAPA Assistant

Guided deviation description, root cause analysis structure and CAPA planning support aligned to EU GMP expectations.

Opening Q3 2026
Risk Management

Risk Assessment Assistant

Structured risk assessment support using FMEA and ICH Q9 frameworks for cannabis manufacturing and quality operations.

Opening Q4 2026

Interested in early access?

ECI AI tools will be available to Professional and Corporate members first. Register interest below.