Learn how to streamline compliance, increase reliability, and reduce costs with a unified automation application.
As life sciences organizations adopt a digital validation solution, they must ensure that it: 1) performs as intended and meets regulatory requirements, 2) prevents excessive documentation and testing, and 3) maintains data integrity throughout its lifecycle.
This white paper describes the capabilities of an end-to-end automation solution, how it simplifies validation, and how it reduces costs in your organization. You’ll also learn why transitioning from a paper-based system to an automation application doesn’t have to be complex and overwhelming.
Download the white paper to explore the possibilities, leverage automation, fuel innovation, and maximize your operational efficiency!
Components of an End-to-End Solution for GxP Systems
Application lifecycle management (ALM) automates regulated workflows like IT change management, provides real-time updates for GxP systems, and helps keep those systems in a controlled state.
Validation lifecycle management (VLM) enables quality and IT teams to mitigate risk and maintain audit-ready records (e.g., periodic reviews) by performing risk assessments and tracking validation efforts at the system level.
Read the white paper and discover how to transform critical compliance workflows into modern and efficient automated processes that minimize your regulatory burdens.
Accelerate Regulated Operations with an Automation Application
Automating and simplifying the validation process helps your organization improve compliance and quality, reallocate resources, and save money. Additionally, automation benefits many regulated IT processes by streamlining the regulatory applicability assessment, GxP IT changes, GxP incident management, user access provisioning, and periodic review.
Know what capabilities to look for in an automation application—download the white paper.
Guidance for Choosing an Automation Application
In today’s resource-constrained business environment, life sciences companies seek greater efficiency in their regulated operations and workflows to reduce risk and cut costs. ProcessX from USDM Life Sciences helps you transition from manual, paper-based processes to an automation application that simplifies compliance and optimizes your existing technology. As a digital accelerator, the benefits of ProcessX include enterprise-wide harmonization of quality processes and automated testing and release management. Specialized GxP services from the most trusted SMEs in the industry modernize your standard operating procedures, audits, and quality assurance processes.
Contact us to learn more about ProcessX, build your business case to show ROI, and drive operational excellence and efficiency in your organization.