Keeping Pharma Manufacturing Running, Compliant and Review-Ready

From Master Recipe to Batch Release

Pharmaceutical teams shouldn’t have to chase spreadsheets, signatures, and system logs to understand what ran, what changed, or why a batch is blocked.

IndX connects product definitions, execution, quality, and supply chain systems so that:

• Approved recipes and parameters reach the line correctly
• Operators execute against enforced process steps
• Deviations are detected and handled in-process
• Batch records are ready for release when production ends

Most delays in pharma aren’t caused by bad manufacturing - they’re caused by slow review and missing context. When execution and quality data live in different systems, teams spend days reconstructing what already happened. IndX eliminates that gap by making the batch record a by-product of running the process.
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IndX works with 19 of the top 20 Pharma companies worldwide

Global pharmaceutical leaders trust us because we operate where pharma execution actually breaks. Across global programs in MES, electronic batch records, serialization, and supply chain compliance, we are trusted to run systems that sit directly in the path of regulatory audits, batch release, and patient safety. Our role is not advisory - we design, implement, and support production-critical platforms that must work every day, across regions, regulations, and product lines.