Disclaimer: AIVF has CE mark. In the US, an AI component of AIVF is considered an investigational device. Limited by Federal (or United States) law to investigational use.
©All rights reserved AIVF 2026

Compliance

At AIVF, we have established and thoroughly tested controls that support your goals in security, privacy, and compliance. Explore how AIVF aligns with a range of regulatory and industry standards to uphold our commitment.

AIVF

Embryology Management Assistant

GDPR

General Data Protection
Regulation

HIPAA

The Health Insurance
Portability and Accountability
System

ISO 27001

Information Security
Management System in Health

ISO 27799

Information Security
Management System in Health

ISO 13485

Medical Devices,
Quality Management System