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Validify automates CSV/CSA compliance for FDA-regulated companies using Salesforce. It turns weeks of manual validation into hours by auto-generating risk assessments and documents, reducing costs and human error. Ideal for pharma, medical device, and other regulated industries.
The Smyte Score is a weighted average from leading review sites across the web.
Significant Time Savings:
Users report that Validify dramatically reduces validation efforts—from hundreds of hours to just 50–60 hours—by automating documentation and risk assessments.
Automated Compliance for Salesforce:
The platform automatically identifies and validates changes within Salesforce environments, ensuring continuous compliance without manual intervention.
User-Friendly Interface:
Customers appreciate Validify’s intuitive design, which simplifies the validation process and enhances user experience.
Limited Integration Options:
Validify currently lacks integrations with other software tools, which could enhance its functionality.
Pricing Transparency:
Some users have expressed a desire for more transparent pricing details upfront to better assess the software’s value proposition.
Customization Constraints:
While Validify offers automation, certain users have noted limitations in customizing validation processes to fit specific organizational needs.
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