# How does Medrio CDMS/EDC ensure compliance, data security, and inspection readiness for clinical trials?

Small to mid-size sponsors and CROs require ironclad data integrity and automated audit trails to mitigate the business risks of regulatory non-compliance and ensure they are always prepared for unannounced inspections.

##### Post Metadata
- Posted at: 5 months ago
- Net upvotes: 1


## Comments
### Comment 1

Medrio EDC is designed to support regulatory compliance and data quality throughout the clinical trial lifecycle. The platform includes validated electronic records and signatures, full audit trails, role-based access controls, and secure data encryption to align with FDA 21 CFR Part 11, ICH E6(R2), HIPAA, GDPR, and other global requirements.

Medrio EDC supports electronic data capture at the point of entry in ways that align with modern eSource expectations, helping reduce reliance on paper documents while maintaining full traceability. Robust data backup, disaster recovery, secure record access, and flexible data exports help ensure inspection readiness and long-term data accessibility.

##### Comment Metadata
- Posted at: 5 months ago




## Related Product
[Medrio EDC](https://www.g2.com/products/medrio-edc/reviews)

## Related Category
[Electronic Data Capture (EDC)](https://www.g2.com/categories/electronic-data-capture-edc)

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