Advanced Research & Regulatory-Compliant Scientific Support
We deliver end-to-end research support for healthcare organizations, academic institutions, and life-science companies. Our expertise spans scientific and medical writing, biostatistics, real-world data (RWD) analysis, and advanced epidemiological modeling.
All research workflows are designed to comply with EU GDPR, German data protection laws (BDSG), and recognized research standards, ensuring data integrity, reproducibility, and regulatory readiness for publication, grant submission, and clinical evaluation.
Custom Health Informatics & Clinical Software Solutions
We architect and develop secure, interoperable, and scalable health informatics systems tailored to the needs of clinics, hospitals, and research institutions. Our solutions support clinical operations, research data management, and digital health innovation while aligning with EU healthcare IT frameworks.
Key capabilities include:
- GDPR-compliant health data processing and consent management
- Interoperability using HL7 and ASTM standards
- Modular architectures for clinical systems, registries, and research platforms
- Integration with existing hospital information systems (HIS) and laboratory systems (LIS)
- Secure cloud and on-premise deployments in line with German hosting and data-residency requirements
Our technology enables organizations to improve efficiency, data quality, and clinical decision-making—without compromising security or compliance.
Professional Training & Digital eLearning in Health Informatics
We provide industry-focused training and eLearning solutions designed to upskill healthcare professionals, researchers, and IT teams. Our programs combine theoretical foundations with real-world application, covering:
- Health informatics and clinical data management
- Research methodology, biostatistics, and evidence-based medicine
- GDPR, data governance, and ethical data use in healthcare
- Digital transformation and health IT best practices in the EU
All training content is aligned with European healthcare regulations, German compliance requirements, and current digital health standards—supporting sustainable knowledge transfer and organizational readiness.
Contact Us
Here’s what you can expect to happen next:
- After reviewing your project’s requirements, one of our experts will get in touch to schedule a call.
- Upon request, we can promptly arrange an NDA to ensure the highest level of privacy.
- You will receive a detailed project proposal with estimates, timelines, and our expert opinion.