Logiserve SA provides services for computer systems in environments regulated by pharmaceutical Good Manufacturing Practice (GMP), including software development, automation engineering, operational support and quality assurance such as computer system validation and audit support.
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Services for computer systems in pharma-regulated GMP environments, including software development, automation engineering, operational support and quality assurance.
Software development
Software development for GMP environments, including user requirements, specifications, architecture and UI design, implementation, testing, commissioning, training, support and maintenance.
Automation engineering
Automation engineering for computer systems in GMP environments, including product selection, risk analyses, specifications, implementation, testing, integration, qualification and project management.
Operational support
Operational support for systems and infrastructure, including system and network administration, hardware services, documentation, plant engineering and process control.
Quality assurance
Quality assurance for computer systems, including CSV and GMP validation, DQ/IQ/OQ planning, audit preparation, compliance assessment and traceability reviews.
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