Why do I need to validate my platform?

In the life sciences industry, where precision, compliance, and patient safety are paramount, software validation is not just a best practice — it’s a regulatory and ethical necessity.

Validation ensures that the software performs as intended, consistently and reliably, under real-world conditions. This is especially critical for platforms used in research, clinical trials, manufacturing, and quality control, as errors can have consequences from regulatory violations to risks to human health.

Seal is committed to ensuring compliance to the most current approach to software validation broadly recognised in the Life Sciences industry. Seal generates and executes the test elements that demonstrate the system is meeting the requirements set for it to function as an electronic quality systems management tool as a standard, integrated part of the product development process.

In Seal, validation has never been easier.

Our validation covers:

1. Baseline platform validation: to verify that Seal functions as expected under controlled, consistent foundation

2. Configuration validation: to verify that the deployed configuration maintains and meets functionality

3. Compliance validation: to verify adherence to relevant industry regulations and standards

https://github.com/opvia/platform/blob/main/docs/public/validation/broken-reference/README.mdhttps://github.com/opvia/platform/blob/main/docs/public/validation/broken-reference/README.md

More questions? Email our experts at [e-mail].