Perfect for study sponsors or CROs in medtech, diagnostics, pharma, biotech and medical devices (ISO13485, CE, MDR, IVDR)
Keep track of recruiting, forms, queries, biosamples.
Intuitive study setup and management. No complex training required.
You can reach us via email or phone. Each study comes with an advanced support plan that fits your needs.
Software that supports your processes
Automated data checks, easy query management and complete, GCP compliant audit trail
Run your trial for FDA clearance or CE marking. Suitable for studies for MDR or IVDR.
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.
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.
Focus on your study and let us handle the software
You own all your data – period.
Our servers are located in Germany. Other locations are available upon request.
GDPR / CE compliant
State of the art encryption: TLS 1.3 and AES-256