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PHARMACEUTICAL MANUFACTURING SOFTWARE

Precision Meets Compliance: Powering Pharma Maintenance at Scale

Stay audit-ready and production-strong with Accruent's EAM solution - purpose-built for pharmaceutical manufacturing compliance and efficiency.

Maximize Operational Efficiency and Compliance

Revolutionize your approach to compliance and elevate operational efficiency with the industry’s most comprehensive EAM solution.

Compliance and Documentation

Accruent’s EAM solution offers a seamless document management system to control and streamline processes, maximizing company-wide collaboration.

Process Efficiency & Automation

Effective digital transformation with robust Computerized Maintenance Management System (CMMS) and IoT technologies is all about having the right functionalities and truly integrated systems.

Data Trustworthiness

Our integrated solution safeguards data and ensures transparency across the organization. Reduce process deviations by ensuring maintenance activities are executed with the latest procedure and approved documents.

Capitalize on the Capabilities that are Transforming
Pharmaceutical Manufacturing

Our platform stands out among EAM offerings with features tailored to strict regulatory standards. It streamlines compliance, automates
maintenance, and generates audit reports, ensuring efficient, compliant operations.

Secure Validation Process

The validation process in pharmaceutical manufacturing ensures product quality and regulatory compliance. Accruent’s secure, validated EAM supports continuous validation and collaboration, keeping engineering content protected and compliance simple, with full visibility and accountability.

Electronic Signatures and Audit Trail Made Easy

Users can easily apply electronic signatures to documents with just a few clicks. With advanced authentication and built-in security features, the solution ensures compliance while saving valuable
time.

Streamlined Procedures Versioning

Ensure procedures are always accurate, current, and audit-ready. Accruent’s EAM turns FDA 21 CFR Part 11 and ISO 27001 from hurdles into enablers. Built-in tools streamline updates, track changes, and link related records for easy compliance.

Automate Calibration and Monitor Asset Health

Streamline calibration with fewer data entry errors, automated work orders, and simplified records. Our IoT monitoring helps reduce time-to-market, detect issues early, predict failures days in advance, and boost compliance.

Actionable Reporting & Analytics

Use configurable maintenance reporting software to analyze key metrics – like work order completion rates or labor costs – address pain points, and make better maintenance decisions.

Control Engineering Content

Fully control your engineering content with version management, secure printing, up-to-date documentation, controlled data changes, and configurable workflows.

How Accruent Powers Smarter Pharma Manufacturing

 

Trusted by 8 of 10

World's biggest pharmaceutical companies

20 + Years

Experience serving the pharmaceutical industry

Up to $1 M

In unplanned downtime costs per batch for pharmaceutical companies

Accruent’s Pharmaceutical Manufacturing Suite

Explore our dedicated Pharma Manufacturing Suite of solutions.

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Multi-site, Multi-Industry CMMS Software

Cut downtime, predict maintenance, automate tasks, stay compliant, and manage equipment inventory with easy-to-use maintenance software.

Maintenance Connection O&G
Meridian dashboard

Meridian

EDMS for Highly Regulated
Environments

Highly customizable on-premise Engineering Document Management Solution (EDMS) built for strict regulatory compliance, with collaborative workflows and tight access controls.

Accruent Observe Logo Small

IoT Remote Monitoring & Energy
Management

Drive operational efficiency, predict asset failures, improve air quality, and
ensure commercial refrigeration compliance with enterprise IoT.

Observe dashboard (3)
abbvie logo

Streamlining FDA Compliance and Audits

“Accruent solution provides us with the tools to maintain FDA 21 CFR Part 11 compliance and ensure current good manufacturing practices, resulting in reduced risks and more streamlined audits.”

— Bill Eager
Drawing Management Senior Engineer

Specialized Solutions for Your Area of Manufacturing

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Pharmaceuticals Companies

Pharma is evolving with biologics, biosimilars, continuous manufacturing, and stricter global regulations. Sustainability, faster vaccine development, and resilient supply chains are now key priorities.

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Bio-Technology Companies

Biologics manufacturing is advancing through digital tools, continuous production for better efficiency and quality, and increased outsourcing—especially in cell and gene therapies.

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Manage Your Pharma Manufacturing, Equipment and Facilities

Frequently Asked Questions

What are the main challenges faced by pharma manufacturers in maintaining compliance?

Pharmaceutical manufacturers face strict regulatory requirements and complex compliance standards. Challenges include managing vast documentation, ensuring process validation, and adhering to critical industry regulations like FDA’s 21 CFR Part 11. Consistent, accurate, and current records are essential to meet these expectations. 

Accruent’s EAM solution ensures maintenance operations are efficient and fully aligned with industry regulations, making compliance easier to manage.

How can pharma companies leverage Accruent’s EAM solutions to manage complex projects?

Pharmaceutical companies can use Accruent’s EAM solution to coordinate complex projects like facility upgrades, maintenance, and product changeovers. Real-time project visibility helps teams stay on schedule and align efforts across departments for seamless execution.

How can pharma manufacturers improve data security with Accruent's EAM software?

Accruent’s EAM software improves data security by providing controlled access for authorized users, real-time updates, and detailed action logs.

These features help maintain transparency, automate version tracking, and create comprehensive audit trails, meeting global compliance requirements and reducing cybersecurity risks.

How does Accruent's EAM solution support compliance with FDA regulations?

Accruent’s EAM solution simplifies compliance with FDA regulations, including 21 CFR Part 11, by offering secure document management and detailed audit trails.

These features ensure that all records are accurate, traceable, and accessible only to authorized personnel, making it easier for pharma manufacturers to meet regulatory requirements and streamline audit processes.

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