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LIMS/ELN Implementation for Global Biopharma

About the Client

The client is a top-20 global biopharmaceutical company operating multiple research and development labs across regions. The organization relied on 15 siloed lab systems, leading to fragmented data, inconsistent workflows, and compliance challenges. Limited integration across instruments and systems impacted productivity and slowed down research outcomes. To streamline operations and ensure regulatory compliance, the organization partnered with Zymr.

Key Outcomes

35% Reduction in Sample Processing Time
50% Faster Audit Preparation

Business Challenges

The organization operated with multiple disconnected LIMS and ELN systems across labs, creating data silos and limiting collaboration between teams. Researchers faced difficulties in accessing unified data, resulting in delays and inefficiencies in sample tracking and analysis.

Manual workflows and lack of automation increased the risk of errors and reduced overall lab productivity. Inconsistent data formats and lack of standardization further complicated reporting and compliance processes.

Regulatory compliance, including 21 CFR Part 11 requirements, was difficult to maintain due to fragmented systems and limited audit trails. Preparing for audits required significant manual effort, consuming valuable time and resources.

The client needed a unified, scalable LIMS/ELN platform that could integrate instruments, automate workflows, ensure compliance, and improve overall lab efficiency.

Business Impacts / Key Results Achieved

Zymr enabled the transformation of fragmented lab environments into a unified digital platform, improving efficiency, compliance, and data accessibility across global labs.

  • 35% Reduction in Sample Processing Time
  • 50% Faster Audit Preparation
  • Improved Data Accessibility Across 15 Lab Systems
  • Enhanced Compliance with 21 CFR Part 11 Standards
  • Standardized Workflows Across Global Research Teams

Strategy and Solutions

Zymr implemented a unified LIMS/ELN platform tailored to biopharma research workflows, enabling seamless integration, automation, and compliance.

  • Unified LIMS/ELN Platform
    Consolidated 15 siloed systems into a single, scalable platform for centralized data management.
  • Instrument Integration
    Integrated lab instruments to enable real-time data capture and reduce manual data entry.
  • Workflow Automation
    Automated sample tracking, processing, and reporting workflows to improve efficiency and reduce errors.
  • Regulatory Compliance Enablement
    Implemented features aligned with 21 CFR Part 11 requirements, including audit trails and electronic signatures.
  • Data Standardization and Accessibility
    Standardized data formats and enabled seamless access across global teams to enhance collaboration.
  • Audit and Reporting Optimization
    Streamlined audit preparation and reporting processes, significantly reducing manual effort and turnaround time.
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