Meridian Cloud for Life Sciences helps you meet regulatory requirements such as Title 21 CFR, cGMP, GMP Annex 11, and other key regulations. It includes features for electronic signatures, audit logs, controlled document editing, and automated watermarks and print stamps.
Release process and validation
Our product release process follows a validated change management approach in a compliant environment. This includes:
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Daily non-functional updates and regular functional releases.
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A time-gap release model between Test and Production tenancies.
This subscription supports your change management procedures and ensures you stay up to date with software upgrades while maintaining compliance from a validation standpoint.
Features exclusive to Meridian Cloud for Life Sciences
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Electronic signature: Verify user identity during review or approval workflows. To use this, enable the Signature watermark type for each applicable document type.
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Test reports: Download daily reports of the automated tests executed in your Life Sciences solution.
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Workflow lockdown: Prevent unauthorized changes to approved or released documents outside of a controlled workflow.
Feature details
Use the following links for more information about the available features:
