The lifecycle of computerised systems in the life sciences industry sector must be appropriately structured and documented, and it is important that your company ensures regulatory compliance.

OdysseyVC offers turnkey project management, validation and documentation services throughout the lifecycle of your computerised systems, as a managed service that lowers risk, reduces overheads and reduces the need for resource management.

Our extensive computerised system validation experience provides your company with leadership on multiple levels, helping Project, Validation and Automation Managers by not just making their jobs easier but providing them with peace-of-mind as well. We do this all while ensuring consistent, best-in-class, audit-ready systems for all of our clients.

Lifecycle Management Services Tailored to Your Needs

For Project Managers

Our unique approach helps us to manage and execute the computerised systems validation element of your project from the concept phase through to retirement as a turnkey solution. This allows you the freedom to oversee the project with the safe knowledge that our unique approach delivers fully validated and audit-ready systems.

For Validation Managers

We provide leadership and clarity around regulation that helps you to manage regulatory compliance. Our proven processes and methods for execution reduce your workload, freeing you and some of your resources up to tackle other projects.

For Automation Managers

Our specialist knowledge and experience working with GxP Computerised Systems means all systems delivered by OdysseyVC will meet strict industry regulatory requirements, providing you with peace-of-mind and making it easier for you to get endorsement from your Validation Manager.