Global Data Governance & Compliance Solutions
In today's interconnected world, life sciences organisations increasingly operate across multiple jurisdictions—conducting multinational clinical trials, deploying digital health solutions globally, and managing cross-border data flows for research and commercial purposes. This global footprint creates significant compliance complexity, as each jurisdiction imposes distinct data protection requirements with varying obligations, enforcement mechanisms, and cultural expectations. iliomad HealthData provides full-spectrum Worldwide Data Protection and Compliance Services, supporting clients with consistent, coordinated privacy programs that span all regions where they operate.
Regional Coverage, Global Expertise
As your global operations expand, so does the complexity of maintaining compliance across multiple jurisdictions with varying requirements. iliomad provides comprehensive worldwide data protection services, ensuring consistent compliance for life sciences organizations operating internationally.
Our expertise across the EMEA region encompasses deep, practical knowledge of the EU GDPR, UK GDPR, Swiss FADP.We coordinate comprehensive compliance programs for organisations handling sensitive personal data, including health records, genetic information, and clinical trial participant data ensuring consistent, rigorous standards throughout this diverse region.
We provide comprehensive support for organisations navigating the complex, multi-layered privacy landscape of NorthAmerica. This includes federal requirements under HIPAA for health information, comprehensive state privacy laws like CCPA/CPRA in California, PIPEDA requirements in Canada, and Mexico's LFPDPPP. Our specialists align these diverse frameworks with GDPR-equivalent standards for unified global compliance.
Our compliance services cover both established and emerging regulatory systems across Latin America, with particular depth in Brazil's LGPD—one of the most comprehensive privacy frameworks in the region.We also support compliance with national data protection regimes in Argentina, Chile, Colombia, Peru, and other Latin American markets, providing operational support for cross-border transfers and regulatory filings.
The Middle East represents a dynamic and rapidly evolving regulatory environment, with several countries introducing comprehensive data protection laws in recent years. We provide specialised support including guidance on the UAE's Federal Data Protection Law, Saudi Arabia's Personal Data Protection Law, Qatar's Data Protection Law, and other emerging frameworks across the Gulf states and broader region.
Our established expertise in the Asia-Pacific region enables us to manage compliance under diverse privacy regimes, including Singapore's PDPA, Japan's APPI, Australia's Privacy Act, India's DPDP Act, andChina's PIPL. We support regional data hosting requirements, data localisation mandates, and transfer assessments ensuring adherence to both local requirements and global standards.
In Australia and New Zealand, our team helps clients align their health data processing, clinical research operations, and digital health deployments with national privacy frameworks while integrating these requirements into unified global compliance programs. We address the specific requirements of Australia's Privacy Act and New Zealand's Privacy Act 2020.
How iliomad Health Data Can Help You
iliomad Health Data has extensive experience managing cross-border regulatory frameworks, ensuring that each project from multinational clinical trials to global digital health platform deployments complies with local, regional, and international data protection requirements while maintaining operational efficiency. Our global network of privacy experts understands local regulatory nuances while maintaining alignment with your organisation's global privacy strategy and business objectives.
FAQs
Our frequently questions
Global data governance is the strategic framework that ensures your organization's data handling practices comply with data protection laws across every jurisdiction where you operate, collect, process, or store data. For life sciences and health tech companies, this is critical: inconsistent data governance creates regulatory exposure, blocks clinical trial approvals, triggers authority investigations, and derails due diligence during fundraising or M&A. Strong data governance reduces legal risk, enables international expansion, satisfies investor requirements, and creates operational consistency across your entire data lifecycle—from informed consent through regulatory submission and long-term retention.
We provide compliance solutions across the full spectrum of global data protection requirements, including GDPR (EU), UK GDPR, HIPAA and FDA data protection requirements (US), CCPA/CPRA (California), PIPEDA (Canada), Privacy Act (Australia), LGPD (Brazil), Turkish VERBİS registration, and jurisdiction-specific frameworks across Asia, Latin America, and the Middle East. With hands-on experience in 66 countries worldwide, we support multinational companies with cross-border data transfer strategies (Standard Contractual Clauses, adequacy decisions, Binding Corporate Rules), adequacy assessments, and compliance readiness for international clinical trials and commercial operations.
Our global data governance services are specifically designed for healthcare, life sciences, biotech, pharmaceutical, MedTech, clinical research organizations (CROs), health AI and digital health companies, and any organization handling sensitive health, genetic, or biometric data across multiple jurisdictions. We specialize in the unique challenges of clinical trial data governance, real-world evidence platforms, patient registries, genetic research, and AI-driven diagnostics where regulatory requirements intersect across borders.
Timeline depends on organizational complexity and maturity. For a focused governance framework covering core data processing activities, expect 6-12 weeks for initial design and implementation. For comprehensive programs across multiple entities, jurisdictions, and data types, plan for 6-12months. We prioritize high-risk areas first getting critical compliance gaps addressed within weeks—while building comprehensive governance systematically. Urgent regulatory deadlines (authority inquiries, clinical trial starts, due diligence) can be addressed on accelerated timelines.
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.
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