Harness the Power of AI in GxP – East 2026 brings together industry leaders, innovators, and compliance professionals to explore the evolving role of Artificial Intelligence in regulated life sciences ...

AI Governance, CSA, Data Integrity, GRC, Risk Management, and Inspection Readiness. Built for FDA-regulated life sciences.

Most staffing firms send bodies. We send domain-vetted life sciences specialists—CSA validators, QA leads, Polarion engineers, and Veeva admins who know GxP, not just coding or project management.

Speak with one of our AI compliance experts and find out how Compliance Group can help your organization adopt and validate AI with confidence.

Score your AI governance and validation readiness across five dimensions in 5 minutes. Get an instant maturity rating and next steps, built to ISO/IEC 42001.

In regulated environments across the pharmaceutical, MedTech, and biotechnology sectors where AI, data integrity has traditionally evaluated through presence, completeness, and traceability of ...

We look forward to meeting you at Booth #109 during the ISPE AI in Life Sciences Summit. Get ready to experience CLAiRE AI Agents and the iQuality Platform in action and discover how AI can help ...

CLAiRE, iQuality, and MAiGRATE are purpose-built for the one constraint generic AI ignores: every claim has to trace back to your organizational truth — not a model's training data. Most life sciences ...

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Medical devices, unlike prescription drugs, are reviewed by the United States (US) Food and Drug Administration (FDA) under one of two regulatory standards - Premarket approval (PMA), which requires ...

There may be some misunderstanding surrounding FDA 21 CFR Part 11 when it comes to regulatory compliance for manufacturers of medical devices. We have discovered a major pitfall here: Many businesses ...