Streamline Software Validation

Software validation doesn’t have to be a painful, time-consuming chore for medical device companies. Validate faster and with less effort using our revolutionary tools and proven processes.

The FDA and other regulators require software validation but don’t specify how it should be done. That uncertainty makes it difficult for medical device and other companies doing business in regulatory environments to meet software validation requirements and expectations.

Don’t worry, though – MasterControl has you covered. Our transformational validation tools and best practice methodologies allow medical device companies to cut validation time from months to days.

Patented validation tools and proven methodologies.
Reduced validation time and effort.
Maintains a continuous state of compliance.

Simplify Medical Device Software Validation

MasterControl’s proven validation methodology significantly reduces the time and effort involved in medical device companies’ validation processes.

MasterControl’s VxT process streamlines validation in the cloud.

The patented Validation Excellence Tool (VxT) drastically cuts testing time and validation burdens.
FDA software validation requires a risk-based approach.

With MasterControl, you can avoid wasting time testing things that don’t affect product quality.
Ensure validation is based on best practices.

We practice risk-based validation according to the latest FDA software validation guidance.
Spend less effort and money on validation.

VxT gives you specifically tailored information based on the MasterControl products you use.
Make validation a sustainable effort.

VxT provides tools and knowledge needed to streamline validation throughout the software life cycle.