Paragon applies its experience in life sciences and technology to helping pharmaceutical firms manage the workflow, content and reporting required for manufacturing and quality processes.
Controlled Content Management
Paragon helps firms adhere to Good Manufacturing Practices (GMP) standards for the preparation, processing and packaging of pharmaceutical products. Paragon has the experience with enterprise content management systems to deliver an automated, integrated online environment for creating, reviewing, revising, approving, distributing and auditing controlled content. Our solutions are built with industry-standard features that include the ability to respond to external regulatory agencies and auditors, enforce signatures and proper approvals, and ensure document retention for required periods.
Standard Operating Procedures (SOP) and Critical Document Management
Paragon provides solutions that deal with the handling of SOP documents, which are critical to defining protocols and good practices for a variety of tasks and processes in the life sciences environment. SOP documents are involved in a number of regulatory processes, and Paragon’s experience with business process management and enterprise content management delivers an integrated approach to efficient workflow and access.
Quickview for Documentum™ Solution
Paragon has developed its own solution to enable Documentum users to search, view, update and approve
SOP documents. The solution includes watermark and e-signature capabilities.
Quality Metrics
Paragon applies decades of experience with business intelligence to deliver management reporting solutions that can minimize exposure with regulatory agancies in the manufacturing process. Paragon knows how to identify the critical KPIs, collect them from various data stores and present them in a portal or dashboard for management consumption.
Case Study: Quality Metrics Portal - Paragon defined, designed and built a Quality Metrics Compliance portal to provide streamlined and timely data capture and visibility into the quality aspects of the client's manufacturing process.