Complete Validation Services
Invensys Validation Technologies services encompass the entire validation project life cycle, including automated systems validation. Services range from the development and implementation of global validation standards to the execution and delivery of project-wide, plant-wide or company-wide validation standards.
Invensys Validation Technologies manages and executes full validation projects, including the development of validation master plans and requirements; GxP Audits, risk management, the development, implementation and execution of IQ, OQ, PQ and 21 CFR Part 11, and other worldwide regulations. We also provide the qualification and validation of process and laboratory equipment, automated and non-automated unit operations, facilities and utilities, as well as computer systems in IT and business.
Our success with clients is due to our knowledge of regulatory issues and how systems, processes, facilities and laboratories work. We manage validation projects completely and efficiently by providing complete supply chain validation services, based on our expertise in:
- cGxP compliance (GMP, GCP, GLP, GDP)
- Research and development
- Clinical manufacturing
- Quality systems
- Operations (manufacturing & packaging)
- All types of computer systems (ERP, MES, IT, DCS, PLC, HVAC, LIMS, etc.)
- Regulatory compliant solutions
Significant benefits can be gained from our expertise in validation methodologies as well as project management and processes. Our highly qualified consultants will help ensure that your operations, policies and procedures and quality systems are in compliance.
Invensys Validation Technologies believes that the operational challenges faced by pharmaceutical and other life science manufacturers require validated solutions designed specifically for them.
