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Pharma Manufacturing

Pharmaceutical manufacturers must adhere to industry compliance standards to introduce products to market faster and in high volumes. With Accruent’s EAM solution, you can be confident that your maintenance operations are not only efficient but also completely in line with industry regulations, mastering compliance demands with ease.

Pharma Manufacturing

Your Comprehensive Solution for 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

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 with Ease

The pharmaceutical industry is subject to constantly changing regulations that impact all stages of the product life cycle. Accruent’s EAM solution offers a seamless document management system to control and streamline processes, maximizing company-wide collaboration, ultimately establishing a ‘single source of truth and ensuring compliance with key industry regulations.

Process Efficiency & Automation

Equipment malfunction and process deviations can lead to contamination or variability in quality. Effective digital transformation and implementation of IoT technologies is all about having the right functionalities and truly integrated systems. This approach assists pharmaceutical manufacturers in meeting essential requirements without disrupting their production processes.

Integrated Solution for Complex Projects

Pharma manufacturers oversee multidisciplinary projects, including facility upgrades, process optimization, maintenance coordination, and product changeovers, while ensuring validated document delivery. Accruent’s integrated solution connects engineering and maintenance departments, providing real-time information to track site, equipment, and documentation status.​

Data Trustworthiness

Our integrated solution safeguards data and ensures transparency across the organization. It automates record processes, like who performed an action and when, simplifying compliance and helping teams identify errors or discrepancies. Reduce process deviations by ensuring maintenance activities are executed with the latest procedure and approved documents.

Security & Safety

Accruent's purpose-built solution extends far beyond a single plant or location, supporting global operations by providing staff worldwide with instant access to accurate, secure, and up-to-date data. Documents are error-free, accessible only to authorized users, and continuously updated, enhancing confidence in compliance and reducing cybersecurity risks.

Prioritization of Mission-Critical Machinery

Pharma companies are prioritizing maintenance tasks based on criticality and impact on operations, emphasizing the importance of preventive measures to reduce failures. Accruent’s EAM solution helps maintenance teams transition from reactive to preventive asset maintenance, extend asset life and facilitate ongoing compliance.

Our Products that Streamline Pharma Manufacturing Operations  

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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

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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.

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. It also tracks information flow, identifies issues, and streamlines compliance tasks, boosting transparency and accountability in the audit trail. 

Streamlined Procedures Versioning

Rest assured that procedures are always accurate, up-to-date, and ready for scrutiny. With Accruent’s EAM solution, regulatory standards such as FDA’s 21 CFR Part 11 and ISO 27001 aren’t hurdles to overcome but frameworks to help your organization to realize its full potential. Out-of-the-box features simplify procedure updates, track progress, and log changes, while quick-access links make it easy to find related records for smooth compliance management.

Secure Validation Process

The validation process in pharmaceutical manufacturing ensures product quality and regulatory compliance. Accruent’s highly secure, expertly validated EAM solution supports continuous validation and secure collaboration, helping businesses stay ahead. It keeps engineering content secure in a compliant environment, making compliance simple, while ensuring visibility and accountability.

Automate Calibration and Monitor Asset Health

Reduce data entry errors, simplify record-keeping, automate calibration work orders, and more for streamlined calibration activities. With our IoT remote monitoring system, you can reduce time-to-market for drugs, use real-time data feeds to proactively detect errors across the value chain, predict and prevent asset failures 3-5 days before they happen, improve regulatory compliance, among other things.

Look under the hood

Learn more about our software, get your questions answered, and find out how it can complement your current technology and processes.

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Integrated Solutions Tailored for Pharmaceutical Manufacturing

Accruent's suite of products works together to provide a comprehensive solution for pharma manufacturers.

Video Walkthroughs

Achieve Compliance Effortlessly with Maintenance Connection CMMS

Streamline time-consuming compliance tasks, improve data and decision-making, boost efficiency, and adhere to the highest regulatory standards.

What is Enterprise Asset Management (EAM)?

Learn what EAM software is and how it helps maximize asset life, reduce costs, optimize operations, centralize asset data, and more.

Operations Made Easy with Seamless CMMS, EDMS, and IoT Integration

Predictive operations are at your fingertips with this CMMS, EDMS, and IoT integration.

Optimize Your Built Environment with Accruent

Understand what your "built environment” is, how to make it run smoothly, and the role Accruent software plays in optimizing operations and maximizing efficiency.

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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Minimize Downtime, Reduce Costs & Future-Proof Your Operations

 

Products Designed to Integrate Your World

Accruent software allows you to fully optimize the lifecycle of your assets and facilities, offering connected workflows, integrated experiences and data-backed insights.