Streamline Pharma Software Validation

Computer system validation doesn’t have to be a painful, time-consuming ordeal for pharma companies. Validate faster and with less effort using our transformational tools and proven processes.

The FDA and other regulators require software validation but don’t specify how it should be conducted. That uncertainty makes it a challenge for pharmaceutical and other companies doing business in regulatory environments to meet software validation requirements and expectations. But there’s nothing to fear – MasterControl has you covered. Our revolutionary validation tools and best practice methodologies allow pharma companies to reduce validation time from months to days – and sometimes hours.

  • Patented validation tools and proven methodologies.
  • Reduced validation time and effort.
  • Continuously maintained state of compliance.

Validation Software for Pharma

Computer system validation doesn’t have to drag on for months. With MasterControl, validation can often be completed in a matter of hours.

  • The most efficient pharma software validation processes in the industry.

    You can save time and effort by taking advantage of the testing and documentation we provide. Our tools and consultants use a risk-based approach to tell you where to focus your computer system validation efforts.

  • A proven computer system validation approach designed for regulatory compliance.

    Our trusted tools and methods have undergone multiple regulatory inspections without a single finding.

  • Revolutionary risk-based validation software for pharma.

    Our patented Validation Excellence Tool (VxT) uses a risk-based approach to tailor validation to your business needs and how you use MasterControl software solutions.

  • Complete computer system validation documentation.

    All the documentation you need to perform a compliant pharma software validation is included with our validation services. This includes your validation plan, transfer operation qualifications (TOQ), transfer performance qualifications (TPQ), installation qualification (IQ) protocols, and the final validation report, among other documents.

  • Experienced computer system validation consultants.

    MasterControl’s seasoned validation experts guide customers through their initial validation effort and prepare them for future computer system validation projects.

Get more pharma software validation info.

Contact us today to learn how MasterControl can simplify your pharma computer system validation processes.

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