Solve your challenges
Promptly resolving quality issues identified in medical devices.
Monitoring and ensuring that suppliers also comply with the requirements of FDA 21 CFR Part 820.
Maintaining up-to-date accuracy of all documentation necessary to demonstrate regulatory compliance.
Achieve excellence in quality control of your medical devices with our software
Adherence to continuous improvement
Ensure process and device quality with a proactive approach to identifying and correcting deviations encountered and required improvements.

Streamlined audit preparation
Simplify the management of all audit stages, from planning to execution, ensuring time and resource savings.

Reduced organizational risks
Identify and mitigate potential risks to medical device safety, protecting both consumers and brand reputation.



Bring this solution to your company
Learn how SoftExpert solutions can help you achieve standards certification and regulatory compliance
Compliance with global privacy and security standards
Advanced data protection
SoftExpert ensures the protection of your company's data and compliance with the requirements of the latest standards.


Integrate with your ERP, CRM, Office365, and much more
Connect SoftExpert Suite to other business tools already used in your organization.
Worldwide Office Locations
Supporting and implementing your growth and expasion everywhere! We are present locally, ready to ensure that SoftExpert solutions are working without limits.
Customize the solution to your needs
Add new modules to your product, customize your experience and get all the solutions you need for your company.

Glossary

An award-winning platform recognized by customers


