The new offering features Qumas’ QDocCompliance and Liquent’s InSight Manager application.
It is designed to provide a centralized, enterprise-wide view of product details, documents and submissions to support collaboration, compliance requirements and the eCTD. It also allows customers to author and edit regulatory content throughout the product lifecycle.
Our new combined solution enables life sciences companies to drastically reduce the time it takes them to bring products to market, said Paul Hands, CEO of Qumas. We have utilized our open systems architecture to bring all the pieces together for an enterprise level compliance solution that addresses submission lifecycle management.
