Odyssey VC releases new Client Story detailing our delivery of a fully compliant digital solution for a leading global specialty biopharmaceutical company.
In our first Client Story, we took you through how Odyssey VC delivered end-to-end computer system validation (CSV) expertise for a global pharma company, ensuring the release of all systems for intended use in line with GxP regulations.
In our latest Client Story, we take you through how we designed and delivered a fully compliant digital solution to facilitate the M&A activity of a global pharma company. The project was an Interim Deviation Management System for a leading global specialty pharmaceutical company in their Biologics Drug Substance Single-Use Commercialisation Facility. The Odyssey VC solution: a fully validated Software-as-a-Service (SaaS) product to manage site deviations as the organisation integrates a former competitor biologics plant into their existing manufacturing network.
With a short timeline & using a Hybrid approach to software development, Odyssey provided one of the fastest fully GxP solutions delivered for this client. In this client story we take you through the process – from the methods we used and the challenges overcome – and through to the outcome and a word from the company themselves.