This guide breaks down the General Data Protection Regulation (GDPR) as it applies to HealthTech innovators who collect, process, or store personal data—especially sensitive health information.
It explains the key principles, legal definitions, and obligations that apply whether you’re operating within or outside the EU, as long as you process EU/UK citizens’ data.
Emphasis is placed on trust, transparency, and privacy-by-design to ensure ethical and legal digital health practices.
What this carousel covers
The scope and enforcement of the GDPR, including penalties and cross-border applicability
Key compliance actions like data mapping, privacy policies, DPIAs, and appointing a Data Protection Officer (DPO)
Specific GDPR obligations relevant to HealthTech: consent, special category data, and the Data Security & Protection Toolkit (DSPT)
Practical resources including the ICO self-assessment, DPIA template, and GDPR compliance checklist
Key takeaways
If your HealthTech product touches UK or EU patient data, GDPR compliance is mandatory—regardless of where your business is based
Conducting a DPIA early and appointing a DPO are essential steps when dealing with high-risk or sensitive data
Good GDPR compliance strengthens user trust, improves NHS procurement readiness, and protects against legal exposure
Data protection isn’t just about technology—it’s about ethics, governance, and building user confidence from day one
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