Pharma & Biotech Industry

Trusted by over 350K Engineering Professionals Worldwide:

Accruent offers regulated companies an out-of-the-box business solution that manages current Good Manufacturing Practices (cGMP) engineering documentation throughout the management of change lifecycle and adds specific features to the core data management engine that help minimize risk, ensure compliance, and avoid costly recalls.

Accruent Solutions for Pharmaceuticals:

• Fully support 21 CFR Part 11 by providing the necessary technical controls
• Support compliance with European Annex 11 of the EU Guide and the Sarbanes-Oxley Act
• Provide a suite of computer system validation templates to support GAMP 5 guidance
• Store data in a central, secure repository with role-based editing and access privileges
• Access the latest as-built information during concurrent projects
• Improve communication throughout the contractor and supplier network
• Integrate with leading technology and CMMS platforms

STREAMLINE AUDITS WITH REDUCED RISK OF NONCOMPLIANCE

• Provide workflows and consistency in business processes across sites
• Reveal audit trails—showing what has changed by who and when
• Enable compliance with life science specific regulations to avoid costly fines and speed time to market

ENSURE FULL CONTROL OF ENGINEERING CONTENT

• Provide version control and revision management in a safe and secure environment
• Ensure proper printing of documents with watermarking
• Guarantee that all users are working on the most current documentation

DELIVER QUALITY PRODUCTS WITHOUT DELAY

• Provide maintenance with accurate documentation while on-site
• Reduce search time for engineering information from hours to minutes
• Avoid production delays due to inaccurate information

ENHANCE COMMUNICATION BETWEEN TEAMS

• Save time by finding key asset information faster
• Provide the same view of official documentation to both engineers and maintenance & operations
• Gain access to markup tools for comments and edits

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