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:
• 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
• 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
• 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
• 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
