Pharma

AI-powered solutions built for GxP compliance

Regulatory compliance shouldn't slow down innovation. Datastack powers paperless digitization with native AI, keeping your operations audit-ready and aligned with US FDA, EMA, and WHO GxP guidelines.

AMS 360

A centralized Access Management System built to simplify, control, and track user access across all GxP-regulated computer systems. AMS 360 streamlines approval workflows, ensures continuous audit readiness, and mitigates security and data integrity risks by maintaining complete visibility over system permissions.

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Mastersheets

A GxP-compliant electronic documentation solution designed to digitize and standardize high-risk spreadsheets used in labs. With time-stamped audit trails, secure electronic approvals, and formula-lock controls, Mastersheets keeps your production and QC records accurate, traceable, and audit-ready.

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ValPro

A unified computer systems validation (CSV) and lifecycle management platform natively built with integrated AI. ValPro centralizes requirement traceability matrices (RTM), risk assessments, protocol execution, and deviation tracking—drastically cutting the time, manual paperwork, and cost associated with recurring validation cycles.

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Pulse IQ

An advanced commercial intelligence solution built for pharmaceutical sales and brand teams. Leveraging extensive IQVIA datasets, Pulse IQ delivers tailored dashboards that reveal market share movements, target prescriber dynamics, and sales performance metrics to elevate your brand's growth.

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V-Connect

A centralized digital platform engineered to modernize vendor and material approval workflows. V-Connect eliminates manual delays, delivers total transparency across every stage of qualification, and minimizes compliance risks—enabling life sciences organizations to make faster, more confident procurement decisions.

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OneView

A unified intelligence platform centralizing data across Sales, HR, QMS, and Manufacturing. OneView delivers complete operational visibility, helping leadership uncover performance trends, mitigate risks, remove bottlenecks, and drive continuous improvement.

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Release with confidence

From 21 CFR Part 11 electronic signatures to automated validation tracking, see how our platforms safeguard data integrity.

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