Since February 2004, AMRI, a company focused on drug discovery, pharmaceutical development, and manufacturing for many of the world's leading healthcare companies discusses has been reaping the benefits of MetricStream'sDocument Management Solution, a proven system for the FDA regulated industry. They have achieved end-to-end automation for management and control for all types of documents such as SOPs, regulatory filings, cGMP and internal quality requirements. In this customer case study, Ashley Peacock, Validation Manager at AMRI discusses building a case for implementing a document management automation by highlighting the tangible costs and risks of the manual system. The presentation also covers MetricStream solution features and key factors leading to MetricStream's selection:
Rich cGMP capabilities with a small footprint
Deep quality management functionality
Multi-site web-based access with central control
Flexibility to meet specific Customer requirements
Low total-cost-of-ownership
MetricStream's understanding of 21CFR Part 11 and cGMPs
To view the recorded webinar, please fill out the form below. For more information, feel free to call us on 650-620-2955/2935 or email us at info@metricstream.com
Panelists
Ashley Peacock
Validation Manager at Albany Molecular - a chemistry-based drug discovery and development company
