Safeguard patient safety, data privacy and system integrity
The healthcare sector is rapidly adopting connected technologies to improve patient care – but with this progress comes new risks. Cyberattacks targeting medical devices and healthcare networks are increasing worldwide, threatening safety, privacy and trust.
Our latest white paper explains how medical device manufacturers and healthcare providers can comply with evolving cybersecurity requirements, with a focus on Australia’s Therapeutic Goods Administration (TGA) regulations and alignment with international standards. It explores current challenges, regulatory expectations and practical steps to strengthen device security throughout the product lifecycle.
What you’ll find in our white paper
- Evolving risks in healthcare cybersecurity
Understand the growing threat landscape, including breaches and vulnerabilities affecting connected medical devices and health data.
- TGA compliance and international alignment
Learn how to meet Australia’s TGA cybersecurity requirements while aligning with global standards such as ISO 14971, ISO/IEC 27001 and IEC 62304.
- Lifecycle approach to device security
Understand why cybersecurity must be embedded across the total product lifecycle – from design and development to monitoring and end-of-life.
- Practical measures for resilience
Explore recommendations to strengthen cybersecurity, including robust risk assessments, secure coding, access controls, monitoring and incident response.
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