We provide experienced IT specialists for pharmaceutical and other regulated environments, combining technical expertise with an understanding of GxP requirements and validated systems.
Our areas of support include:
- Computerised System Validation (CSV), including requirements, testing and documentation
- ERP, manufacturing, laboratory and quality applications
- System implementations, upgrades, integrations and data migrations
- Change control, impact assessments and validation documentation reviews
- IT transitions supporting acquisitions, divestments and business separation
- Project management and coordination across IT, Quality and business teams
Whether you need an individual specialist or additional project capacity, we tailor our support to your systems, quality framework and delivery requirements.