IGOR safeguards your research data while supporting compliance with regulatory guidelines. So your team can work with confidence, no matter where science takes you.

We use industry-leading cloud infrastructure and modern security best practices to ensure your data is protected.
IGOR is built to support 21 CFR Part 11 compliance, helping regulated teams manage electronic records and signatures with confidence.


For research organizations in the UK, IGOR supports compliance with the Human Tissue Authority (HTA) by providing full traceability of human tissue samples - from arrival on-site through to disposal. The same rigorous tracking and audit features also support the safe handling, documentation, and disposal of hazardous materials in line with institutional and regulatory requirements.
IGOR supports your SOP-driven workflows and standardized data capture - helping you stay compliant with GLP and GMP expectations. From creating reusable experiment templates to managing SOP approval workflows, IGOR helps you maintain consistent processes and high data standards across your entire organization.


As a cloud-based platform trusted by research teams around the world, IGOR puts data protection and privacy at the core of everything we do. We implement privacy and security best practices that meet the needs of biotech, pharma, and academic teams handling sensitive scientific and personal data.
From the FDAâs GLP, GMP, and 21 CFR Part 11 to the HTA and EMA, the regulatory landscape can feel overwhelming. IGOR helps your team navigate it with confidence.
More than just an ELN, IGOR includes built-in safeguards like role-based access, audit trails, digital signatures, and SOP management - plus streamlined workflows that make documentation and approvals part of your everyday process.
Your team is responsible for compliance - but IGOR gives you the tools to make it manageable, reliable, and part of your everyday lab operations.
SOP Management
Create, share, and manage standard operating procedures within your lab workflows - a must for regulated environments.
21 CFR Part 11 Compliance
Digital signatures, audit trails, and access controls to meet FDA requirements for electronic systems.
GLP & GMP Support
Built-in SOP management, experiment templates for standardized data capture, and detailed audit trails support GxP.
Version Control & Data Integrity
Maintain transparent records across experiment iterations and protocol changes, without data loss.
Review & Approval Workflows
Maintain transparent records across experiment iterations and protocol changes, without data loss.
GDPR Compliance
Maintain transparent records across experiment iterations and protocol changes, without data loss.
Let us show you how easy lab data management can be.
