

Building a Secure GenAI Architecture in HealthTech: Avoiding HIPAA & GDPR Pitfalls
Learn how to build secure GenAI architectures in HealthTech. Avoid HIPAA/GDPR pitfalls with identity, data, and compliance guardrails.

Sekurno
Sep 5, 202527 min read


How Can Generative AI Be Used in Cybersecurity: Opportunities, Risks & Tools
How can generative AI be used in cybersecurity? Practical uses in pentesting/AppSec, compliance automation, key tools, risks (phishing, prompt injection), and best practices.

Sekurno
Sep 3, 20256 min read


Biotech Cybersecurity Report 2025: Inside the Exposure of DNA and Health Records
Discover what we learned analyzing 50 biotech companies in 2025 — including critical cybersecurity risks like insecure APIs, leaked credentials, and misconfigured environments. This report highlights real-world threats to genomic data, HIPAA/GDPR compliance, and patient trust, with practical steps for biotech and healthtech teams to improve their security posture.

Sekurno
Jul 31, 20253 min read


GDPR and Cybersecurity in Biotech: How to Protect Genetic & Health Data in the EU
As biotech and healthtech companies scale across borders, they face a central challenge: how to lawfully collect, store, and use ...

Kristina Romanenko
Jul 29, 202512 min read


ISO 27001 Compliance: Checklist & Guide for Biotech & HealthTech Companies
Biotech companies are under pressure to prove strong data security and compliance. This practical ISO 27001 guide and checklist outlines what biotech firms need to know in 2025 — from protecting IP and clinical data to choosing the right auditor and reducing risk.

Kristina Romanenko
Jul 10, 202511 min read


MDR Cybersecurity Compliance: Complete EU MDR/IVDR Compliance Guide & Checklist for Medical Devices
Navigating MDR cybersecurity compliance under the EU’s new medical and in vitro diagnostic regulations can be complex. This in-depth guide helps device manufacturers understand and implement the cybersecurity requirements of EU MDR (2017/745) and IVDR (2017/746) — from secure-by-design principles to post-market surveillance and CE certification. If you're building or selling connected medical devices or software in Europe, this is essential reading.

Kristina Romanenko
May 28, 202512 min read