Magana Trial Manager

Industry

Perfect for study sponsors or CROs in medtech, diagnostics, pharma, biotech and medical devices (ISO13485, CE, MDR, IVDR)

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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.

Be safe

Security Features

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

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