Automated Software Validation for Life Sciences

Accelerate your Software's Time-to-Value &

Lower your Compliance Risks

The Problem with Traditional Validation

Manual validation methods in life sciences are slow, error-prone, and can’t keep up with evolving regulations. Critical systems like QMS, LIMS, MES, and ERP require frequent updates—putting pressure on teams to validate and maintain compliance without delays.

- Time-Consuming – Manual validation testing and high volume of document creation drag out validation cycles
- Error-Prone – Increased risk of mistakes, rework, and audit findings
- Hard to Scale – Frequent updates overwhelm internal teams

Power Your Validation Plan with Automation

SIMCO automates the most time-consuming phase of validation —test execution. Our services-based solution allows the creation & execution of test scripts aligned with your requirements and risk assessments, delivering faster results and cleaner compliance.

- Automated Execution – Runs test cases based on your validation plan
- Structured Results – Generates clear, audit-ready documentation
- Built for Reuse – Simplifies future updates with reusable script executions
- Track project progress - Track every stage of your validation document creation & Test Execution phases

man looking at validation reports on screens

Key Benefits of Automated Software Validation

SIMCO’s solution helps life sciences teams cut validation time by up to 93%, reduce costs, and stay audit-ready — all while meeting regulatory standards. Automate the entire validation lifecycle, from documentation to Performance Qualification (PQ) test execution, so you can focus on innovation, not paperwork.

- 93% Faster Validation Test Execution – Eliminate manual effort, errors and rework
- Expert PQ Support – Validate customized workflows with confidence
- Undisputed Audit Preparedness – Get complete, standards-compliant documentation every time

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Validation You Can Trust. Proof You Can Show

SIMCO’s Automated Software Validation delivers fast, compliant validation with clear, audit-ready documentation. Every test cycle generates structured records to satisfy both regulators and internal quality teams—giving you confidence at every step.

- Audit-Ready Reports – Summary results with digital signatures for fast inspections
- Detailed Test Evidence – Step-by-step logs with screenshots and video for full traceability
- Reusable Scripts – Pre-built automation ready for future updates and re-validation

Supports leading SaaS Software Apps

Run Automated validation tests for PQ workflows for the top industry SaaS software applications including QMS, ERP, LIMS, CRM, Document Management Systems, and many more. Ensure faster, error-free validation cycles with test libraries tailored to each application.

Expert Validation Documentation, Done for You

Beyond automated test case execution, SIMCO delivers complete validation documentation services—crafted by industry experts to meet regulatory standards. From planning to traceability, we help you build a compliant, audit-ready validation package with confidence.

We develop:

- User Requirements Specifications (URS)
- Validation Plan & Risk Assessment
- Test Cases
- Traceability Matrices