Welcome to our blog, your go-to resource for the latest insights and trends in the life sciences industry.
Our blog is designed to provide expert guidance, practical tips, and thought leadership on key areas like medical device development, digital health, and clinical trial optimization. We cover a wide range of topics, including decentralized clinical trials (DCTs), the integration of digital health technologies (DHTs) in DCTs, and the use of Platform as a Service (PaaS) in medical device software development, to help you navigate the complex intersection of innovation and regulation. Our goal is to keep you informed and equipped with the knowledge needed to overcome industry challenges, drive innovation, and succeed in the rapidly advancing life sciences sector. Explore our blog for in-depth insights and the latest developments, and feel free to reach out if you need further assistance.
Categories:
- Clinical Research
- Cybersecurity & privacy
- Data Integrity
- Device Validation & Usability
- Digital Health
- Digital Health Technologies
- Digital health Technology
- Digital Transformation
- General
- Innovation
- Logistics
- Medical Device Software Development
- Quality Management
- Regulatory
- Risk-Based Quality Management
- Usability
- Usability Testing
- Validation
The May 2026 EUDAMED Deadline: What It Means for Digital Health Technologies in Clinical Trials
Is your wearable sensor registered in EUDAMED — and does it need to be before 28 May 2026?
What happens to your EU clinical trial if the device manufacturer doesn't have a Single Registration Number?
Does your SaMD vendor know that EUDAMED registration is now a prerequisite for CE marking?
Are you prepared for the Clinical Investigations module to go mandatory with zero voluntary phase?
Could your next GCP inspection flag a EUDAMED registration gap you didn't know existed?

