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Healthcare & Medical Technology
Industry focus
Clinical data carries clinical risk.We govern it accordingly.
Hospitals, clinics, digital-health platforms and device makers handle some of the most sensitive information there is, often across provincial and international borders.
We structure consent, secondary use, research collaborations and vendor arrangements so that care and innovation are not slowed by avoidable legal uncertainty.
Our Differentiator
Health information law is not a template exercise.
We work with clinical, product and security teams to map data flows, define lawful bases for use and document decisions in a way that survives audit and ethics review.
For connected devices and clinical software, we align privacy, cybersecurity and product obligations before submission and deployment.
- Health Information
- Consent & Secondary Use
- Medical Devices
- Research Collaborations
- Cybersecurity
Our Added Value
Data mapping
We document clinical and operational data flows and the rules that attach to each.
Consent architecture
Consent, authorization and de-identification strategies for care, research and analytics.
Device & software
Privacy and security requirements built into connected devices and clinical software.
Breach readiness
Playbooks that account for clinical continuity, not only legal notification.
Who It’s For
- Hospitals, clinics and care networks
- Digital-health and telemedicine platforms
- Medical device and clinical software manufacturers
Our Team of Experts
Ceiba Law relies on a team of experts who specialize in their respective fields to provide you with the best advice.
View the complete team
Managing Partner
Vanessa Henri, LL.M.
Key services
Software Development
AI and Information Services
Partner
Elodie Meyer, LL.B.
Key services
Finance & Insurance
Education & Public Institutions
Partner
Shawn Ford, LL.M.
Key services
Healthcare & Medical Technologies
Finance & Insurance