Inspired by innovation
We connect science, technology, and people to transform the way care is delivered. We integrate clinical research, digital health, regulatory solutions, and telemedicine into one connected ecosystem to make care smarter, safer, and more accessible for everyone.
Our Ecosystem
One vision. Endless connections.
We4 Clinical Research
A full-service Contract Research Organization (CRO)
combining scientific rigor and digital tools to accelerate compliant, patient-centered clinical studies.
We4 Regulatory
Your regulatory and compliance partner, guiding MedTech and Digital Health companies through MDR, IVDR, and SaMD certification with confidence.
We4 Digital Health
Developer of connected platforms and customized medical devices for remote monitoring and therapy management.
We4 Events
A hub for education, healthcare training, and scientific exchange, blending technology and engagement.
55+
Clinical Trials
600+
Investigators
300+
Hospitals
16k+
Patients
What’s slowing you down?
At We4, we combine proprietary technologies, clinical research expertise, and regulatory know-how into a single ecosystem.
This allows us to move faster and more smoothly, without compromising quality, data integrity, or compliance.
Are your clinical trials delayed by complexity and compliance pressure?
→ Discover how we support compliant, efficient trials
Do you need to collect, manage, and connect health data securely?
→ Explore our Digital Health ecosystem
Struggling to keep up with MDR, IVDR, SaMD, and evolving regulatory expectations?
→ Navigate regulation with confidence
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What makes us different
Innovation is powerful when it’s structured. We combine cutting-edge technology, clinical discipline, and regulatory accuracy to accelerate progress across the health ecosystem.
- Integrated platforms
Our interoperable solutions are designed for the digital transformation of healthcare systems — combining performance, security, and full compliance. - Proprietary technology
We operate on a scalable proprietary tech stack supported by a SaaS model, enabling rapid time-to-market, adaptable integrations, and sustainable growth. - Compliance-first mindset
Fully aligned with EU & US standards (GDPR, MDR, HL7 FHIR, SaMD certification), ensuring every innovation meets the highest global benchmarks. - Clinical network
A unique blend of medical, technical, and regulatory experts, working side-by-side with CROs, hospitals, and research institutions to co-develop reliable solutions.
We4 Healthcare News
Latest insights from the
We4 ecosystem
Healthcare partners expect proof, not promises. We focus on measurable outcomes, real‑world deployments, and transparent learnings from our projects.
MDR – Racing Against Time for Your CE Mark
The extension is here, but it’s not a safety net. Learn how to move fast, stay compliant, and protect your market share. With Regulation (EU) 2023/607, the European Commission has introduced a critical extension to MDR deadlines for legacy devices certified under the previous MDD (Directive 93/42/EEC). It’s a valuable opportunity—but not an excuse to delay.…
GCP R3 – Episode 1: What you need to know (Especially if you work in MedTech)
GCP R3: GCP is evolving, are you? The ICH has released the E6(R3) revision of Good Clinical Practice (GCP), and it marks a turning point. With this update, the rules of clinical evidence have changed, and if you’re working on medical devices, SaMD or digital health, you’re in the game now too. No need to worry, here’s a…
Talk to our Experts
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