Pharmaceutical manufacturing operator holding tablet

MES for for Pharmaceutical Manufacturing

Audit-ready. Easily validated. Built for change.

Streamline compliance, reduce release delays, and digitize batch records with a flexible MES made for regulated pharmaceutical operations.

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  • Operator-first, GxP-aligned

    Empower frontline teams with intuitive, compliant digital tools that reduce human error and review cycles.

  • Fast implementation, faster ROI

    Go live in 90 days with validated digital workflows, built to simplify audits and reduce paper overhead.

  • Composable, not rigid

    Built for pharma: no-code, cloud-native, and ready to integrate with QMS, LIMS, and ERP systems.

  • Validation-grade, audit-ready

    Includes audit trails, e-signatures, and access controls—all pre-configured to support 21 CFR Part 11 compliance.

Join Top Manufacturers

Across manufacturing, companies are transforming their operations with Tulip.

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.

Worker setting up a packaging line for pharmaceuticals

  • 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.

  • Adapt at the speed of regulation

    Update SOPs, logbooks, and batch records in days, not months without custom coding or endless change requests.

  • Modernize without disruption

    Deploy app-based solutions alongside existing QMS, LIMS, or ERP systems. Validate quickly, iterate fast, and scale only what works.

Recognized leader in frontline operations

  • G2 Leader 2024
  • Leader IDC Marketscape 2024-2025
  • 4.5 rating on Gartner Peer Insights 2024
  • Challenger MES 2021, 2022, 2023
pharma factory

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.

Explore Tulip's Composable MES

Advantages of composable MES

  • 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.

  • Fast, Iterative Roll Out

    Replace all-or-nothing MES deployments with modular, validated apps you can deploy, adapt, and scale in weeks.

  • Open and Extensible

    Integrate with your LIMS, ERP, historians, and equipment with Tulip’s open API and pre-built connectors.

  • Flexible, Validatable Data Model

    Track every batch, material, and action with a data model built for compliance and adaptable to any pharma process.

  • Democratized Development

    Enable process and quality engineers to build compliant apps with no-code tools with IT oversight and centralized governance.

  • Modern Architecture

    Leverage AI, connected devices, and automations to build digital workflows that streamline compliance and improve operational performance.

Stock_Photo_Life_Sciences_21 - glass vials

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.

Read the Case Study
Frequently Asked Questions
  • What makes Tulip a leading MES solution for pharmaceutical manufacturers?

    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.

  • How does an MES help manufacturers digitize batch records?

    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.

  • Does Tulip’s MES support GxP and 21 CFR Part 11 compliance?

    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.

  • How quickly can a pharma company implement a composable MES?

    Traditional MES deployments can take years. Tulip’s pharma MES can be implemented in as little as 90 days with validated apps for logbooks, weigh & dispense, sampling, packaging, and eBR review — allowing manufacturers to see ROI in months, not years.

  • Can pharma manufacturers integrate MES with existing QMS, LIMS, and ERP systems?

    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.

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