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Digital health, data and cybersecurity

Our dedicated team of digital health and regulatory affairs professionals is here to support you from medical software development and data management to regulatory planning and quality assurance.

Digital Health Services

The global digital transformation of healthcare brings with increase of software as a medical device or as part of a device, possibly involving AI, IoT, mobile apps, or telemedicine. At the same time, there are growing regulatory requirements for medical software and health data management, along with information security concerns. We help medical device developers to tackle these challenges.

Our in-house digital regulatory experts and medical software developers understand digital health solutions; we understand the development process and foresee risks associated with the digital medical landscape while adhering to local and global data protection and regulations.

Cybersecurity

Cybersecurity in medical devices is critical given the increasing integration of software and connectivity in healthcare technology. Many regulatory agencies have therefore focused specifically on this area with outlined regulatory requirements on cybersecurity and data privacy.

We can support building Quality Management Systems that include cybersecurity considerations:

  • Threat identification
  • Risk assessment
  • Secure design and development
  • Authentication and access control
  • Data protection
  • Updates and patch management
  • Network security
  • Incident response planning

Explore our services

Regulatory and Quality Assurance services

  • Regulatory planning in line with EU, FDA, or any other regulation to ensure your product meets all the requirements
  • Creating software development environments that can be connected to your Quality Management System (QMS)
  • Building an Electronic Quality Management System (eQMS) such as scilife.io
  • Integration of Jira/Confluence workflows into your electronic QMS (eQMS)

Development services

Platform services

  • Setting up cloud environments (development/production)
  • Modifying Jira/Confluence to support medical device development

Contact us for more information

Meeri Säily
Meeri Säily
Sales Director

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Latest news

Read the latest news from the world of quality.

QAdvis and Scandinavian CRO join Aurevia to strengthen clinical research and regulatory expertise

Scandinavian CRO (SCRO) and QAdvis will now operate under the name of Aurevia.

Meet us at ESCMID 2025 in Vienna

We will be at the ESCMID 11-15 April 2025 in Vienna, Austria.

Aurevia appoints Jonna Pelanti as the new Head of EQA business area

We are delighted to announce the appointment of the new Head of the EQA business area Jonna Pelanti.
Meet us at BioMedica in Dublin on 18-20 March.

Meet us at BioMedica in Dublin

Meet us at the BioMedica exhibition at booth A18!

Aurevia appoints Ulrika Hammarström as the new Head of CRO business area

We are delighted to announce the appointment of the new Head of the CRO business area Ulrika Hammarström.