Thanks to our expertise in the pharmaceutical sector and Certified Information Systems Auditors (CISA),we offer you solutions to have confidence in your computerised system validation processes with a high degree of assurance.
Our strategy involves project management and the related documentation with a risk based approach of all components of a system.
By using our experience in several projects and our regulatory knowledge we assure the quality in your computerised system, equipment, facilities during the lifecycle phases to ensure compliance with the requirements specifications
Validation includes inventories and master plan, risk assessment, plan, validation activities, validation reports, change management, on-going evaluation, SOPs, training...
Our computerised system validation methodology helps to assure quality by minimising the risk of errors and system failures, gives you a framework for management control of complex computerised systems in order to lower the maintenance and support costs through the systematic use of project and quality standards.
We are invading your company to restore it brand-new with our ultimate efficiency.