Compliance Solutions for Life Sciences.
Worldwide.

iliomad provides specialized regulatory compliance and data protection services for life sciences companies. We help biotech, pharma, MedTech, and health AI companies navigate GDPR, clinical trial compliance, EU AI Act requirements, and cross-border data protection so you can focus on innovation while staying audit-ready.

We're regulatory compliance specialists, not lawyers. While law firms provide legal opinions, iliomad delivers operational implementation. We act as your external DPO, build compliance frameworks, and prepare you for audits and due diligence practical solutions that regulators and investors expect to see working in practice.

We provide worldwide regulatory coverage with hands-on experience in 75+ countries. Our core expertise includes GDPR for clinical trials, EU AI Act compliance, FDA data protection requirements, HIPAA, and international data transfer mechanisms (Standard Contractual Clauses, adequacy decisions). Beyond the EU and US, we handle country-specific requirements including Turkish VERBİS registration, Canadian PIPEDA, Australian Privacy Act, and jurisdiction-specific obligations across Asia, Latin America, and the Middle East.

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Absolutely. Clinical trial compliance is core to our practice. We help sponsors, CROs, and sites navigate informed consent requirements, cross-border patient data transfers, investigator agreements, and regulatory submissions to ensure your study meets both scientific and data protection standards.

We typically begin with an initial assessment within one week of engagement. For urgent regulatory matters—such as authority inquiries, clinical trial blockers, or due diligence preparation we can mobilize immediately to address critical compliance gaps.

Contact us through our website form or email directly. We'll schedule an initial consultation to understand your regulatory landscape, identify immediate priorities, and propose a tailored engagement that fits your timeline and budget.