Industry

Perfect for study sponsors or CROs in medtech, diagnostics, pharma, biotech and medical devices (ISO13485, CE, MDR, IVDR)
Clean Dashboard
Keep track of recruiting, forms, queries, biosamples.
Easy and Intuitive
Intuitive study setup and management. No complex training required.
Free support
You can reach us via email or phone. Each study comes with an advanced support plan that fits your needs.

Industry Advantage

Software that supports your processes
Online Query Management
Automated data checks, easy query management and complete, GCP compliant audit trail.
Compliant with all regulatory requirements
Run your trial for FDA clearance or CE marking. Suitable for studies for MDR or IVDR.
Unlimited Multi-Center and Multi-Language Capabilities
Magana's intuitive but powerful user management gives you complete control – especially in multicenter studies with many study nurses and researchers. Design different language versions of your CRFs but view the results in the language of your choice.
Easy User Management
Be in control of what your users can do. Create, delete and manage users with different permissions such as study physicians, study nurses, data managers or clinical monitors. Audit trail included.

Security Features

Easy, secure, GCP compliant
You own all your data – period.
GDPR / CE compliant
Our servers are located in Germany. Other locations are available upon request.
State of the art encryption: TLS 1.3 and AES-256