SeerPharma’s Software Solutions team has been engaged to implement an electronic Quality Management System (eQMS) for a major multinational pharmaceutical company.
The team will move the client’s existing Documents, Training and CAPA systems in to an electronic QMS platform to help with process efficiency, transparency and archiving. SeerPharma will also develop and configure a solution to manage the client's Audits, Suppliers and Risk functions.
Once configured and deployed, our team of Computer System Validation (CSV) specialists will help validate the solution to ensure that it complies with relevant TGA (PIC/S) and US FDA requirements.
The project builds on SeerPharma’s extensive experience of deploying, validating and supporting eQMS solutions to clients in the Asia-Pacific region.
Contact us should you be interested in implementing or validating an electronic Quality Management System solution in your organisation.
This post comes from our October 2016 Journal. You may also be interested in these posts:
