Building regulated mobile apps for Heidelberg's life sciences ecosystem. From DKFZ to pharma giants, we create compliant digital health and research applications.
Regulated mobile solutions for Heidelberg's pharma, biotech, and research sectors.
Real results from Heidelberg's pharma companies, biotech startups, and research institutions.
We use validated technologies that meet pharmaceutical and medical device requirements.
Cross-platform iOS and Android
Google's UI toolkit
Native iOS development
Native Android development
Scalable backend
German data residency
Healthcare data standards
Rapid MVP development
Validated development for pharmaceutical and medical apps.
Healthcare data standards for interoperability.
AWS Frankfurt hosting for health data requirements.
Support for BfArM, FDA, and notified body submissions.
Native speakers who understand academic and pharma culture.
On-site meetings at your Neuenheimer Feld or campus office.
Our validated methodology for building compliant life sciences applications.
We analyze your compliance requirements including GxP, DiGA, MDR, and define a validated development approach.
User-centered design with proper documentation for regulatory submissions and validation protocols.
Development following GAMP 5 principles with proper change control, testing, and documentation.
IQ/OQ/PQ validation protocols, security testing, and compliance verification for regulatory submissions.
Documentation for FDA, BfArM, or notified body submissions with ongoing compliance maintenance.
Ready to build a compliant life sciences or digital health app? Get in touch with our regulated industries team.
21 CFR Part 11 and GAMP 5 validated development.
Deep expertise in pharma, biotech, and research.
Experience with BfArM certification process.