Composable MES for Pharma
Replace paper, simplify compliance, and tailor digital workflows for every cleanroom process, from weigh & dispense to eBR review. Tulip’s composable MES makes it easy to standardize, scale, and validate apps without slowing operations.
Recognized Leader in Frontline Operations
Pharma Manufacturing Demands Composability
Traditional MES slows you down. Every change requires costly validation, vendor involvement, or lengthy change control. Tulip gives you modular, compliant building blocks to digitize batch records, scale processes, and adapt quickly to regulatory shifts.

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Support every GxP role
Operators get guided workflows, QA gets real-time traceability, and IT gets governance, all in one system that scales without silos.
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Adapt at the speed of regulation
Update SOPs, logbooks, and batch records in days, not months without custom coding or endless change requests.
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Modernize without disruption
Deploy app-based solutions alongside existing QMS, LIMS, or ERP systems. Validate quickly, iterate fast, and scale only what works.
Advantages of Composable MES
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Human-Centric
Create workflows that are easy to use, compliant by design, and built with the operator in mind. Integrate AI copilots to reduce training time and guide execution.
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Fast, Iterative Roll Out
Replace all-or-nothing MES deployments with modular, validated apps you can deploy, adapt, and scale in weeks.
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Open and Extensible
Integrate with your LIMS, ERP, historians, and equipment with Tulip’s open API and pre-built connectors.
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Flexible, Validatable Data Model
Track every batch, material, and action with a data model built for compliance and adaptable to any pharma process.
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Democratized Development
Enable process and quality engineers to build compliant apps with no-code tools with IT oversight and centralized governance.
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Modern Architecture
Leverage AI, connected devices, and automations to build digital workflows that streamline compliance and improve operational performance.
Case Study
Pharmaceutical company leveraged apps to reduce line changeover time from 14 days to 3.
See how digitizing SOPs for a complex equipment line changeover reduced errors and time to complete. As the operation progresses, applications automatically update and provide visibility on challenges and timelines.
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Tulip is recognized by Gartner, Forrester, and customers as a top MES for regulated industries, with consistent leadership rankings on G2 for ease of use, speed to value, and customer satisfaction. Unlike traditional monolithic systems, Tulip’s composable MES enables pharmaceutical manufacturers to digitize electronic batch records, logbooks, weigh and dispense, and sampling with apps that are simple to validate and adapt.
Built with GxP and 21 CFR Part 11 in mind, Tulip includes audit trails, electronic signatures, access controls, and integrations with ERP, QMS, and LIMS. This combination of agility, compliance, and usability helps manufacturers reduce release delays, stay inspection-ready, and maintain end-to-end traceability without the disruption of legacy MES deployments.
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Manufacturing execution systems help manufacturers digitize batch records by automating data collection electronically instead of on paper. These systems help enforce steps, captures what happens during production, and keeps a record you can trace back. That makes it easier to catch issues early, finish reviews faster, and stay compliant.
The problem is, most MES systems are hard to change. Tulip is built differently. It gives teams the tools to design their own workflows, pull data from equipment, and see what’s happening on the line as it happens. That kind of flexibility matters when processes change often or the rules keep shifting.
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Yes. Tulip’s platform is validation-ready and supports GxP-regulated environments. It includes audit trails, electronic signatures, access control, and secure data handling to meet 21 CFR Part 11 and Annex 11 compliance requirements out of the box.
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Yes. Tulip’s open API and connectors make it easy to integrate MES apps with existing QMS, LIMS, ERP, historians, and lab equipment. This ensures end-to-end traceability and eliminates data silos across pharmaceutical operations.
Apps Make Operations Better
See how composable MES accelerates validation, reduces review time, and empowers your frontline.