Streamlined Compliance in
Regulated Environments

2025

AI Health Apps. More Than Just Wellness Tools

Intended Use under MDR

Is My Software a Medical Device?

Software Medical Device Classification

Post-Market Surveillance for Healthcare Software

Risk Management for Healthcare Software

QMS for Healthcare Software

Choosing the Right Standard for your Healthcare Software

Data Protection for Medtech Startups

2024

CE Marking for Medical Device Software

Wearables, Skepticism and Data Privacy

Innovation vs Regulation

Privacy Policy versus Privacy Statement

Data Leak vs Data Breach. Differences Explained

California Consumer Privacy Act

FDA’s Approach on Remote Patient Monitoring Devices

Do I need a Privacy Notice?

When Is a DPIA Necessary? A Guide for Businesses

Medical Data Privacy

CE Mark and FDA Approval for Medical Devices

Minimization, Pseudonymization or Anonymization?

GDPR versus CCPA

Health Insurance Portability and Accountability Act (HIPAA)

Canada’s PIPEDA

LGPD Data Subject Rights

Brazil’s General Data Protection Law (LGPD)

GDPR Legal Grounds for Processing Personal Data