Standardized Compounding, Powered by Software

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PARTNERSHIP

Compliant Digital Workflows For Non-Sterile Compounding

Select validated formulations or create your own, execute standardized compounding workflows with integrated QC steps, and generate audit-ready digital batch records, supporting USP <795>-aligned non-sterile compounding.

CurifyLabs Create: Personalization Without Limits

CurifyLabs Create expands our already validated Formulation Library with your own patient-specific formulations. You can now design and formulate from pure APIs or crushed tablets, producing various dosage forms freely with our technology and excipient bases.

This software feature empowers you to design custom formulations faster than ever. Unlock new therapies and elevate patient care: your creativity becomes your competitive advantage.

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Digital Batch Records & Full Traceability

Aligned with 21 CFR Part 11, Annex 11, and standard pharmacy documentation requirements. All compounding data (inputs, parameters, checks, results) are stored automatically in a secure digital batch record.

No more handwritten logs or fragmented spreadsheets, but instant audit readiness and full traceability from raw materials to the final dose.

Digital Batch Records & Full Traceability

Aligned with 21 CFR Part 11, Annex 11, and standard pharmacy documentation requirements.

All compounding data (inputs, parameters, checks, results) are stored automatically in a secure digital batch record.

No more handwritten logs or fragmented spreadsheets, but instant audit readiness and full traceability from raw materials to the final dose.

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