We standardize laboratory instrument PCs and related hardware in line with current IT and compliance requirements.

For software and applications, we apply the same structured approach, ensuring alignment with GMP expectations and 21 CFR Part 11 requirements where applicable.

All implementation steps are fully documented to ensure end to end traceability, audit readiness and reliable day to day operation in regulated laboratory environments.

Core Services

• Setup and standardization of instrument PCs in line with defined guidelines, including guideline development where required
• Installation and configuration of applications in accordance with GMP and 21 CFR Part 11 requirements
• Full documentation of all tasks and activities to ensure controlled, compliant operation
• Structured implementation of applications supported by validated processes and lifecycle controls