Emerson DeltaV™ uses a Digital Control System (DCS) to manage and control all process phases and parameters, while ensuring supervisory control and data acquisition functions.
Developed in accordance with globally shared DeltaV™ standards and featuring a unique range of capabilities (secure data recording, advanced analytical tools, trend and historical data management, S88-compliant batch control, operator access management, alarm management, maintenance functions, etc.), this solution is ideally suited for the implementation of complex, multi-equipment industrial processes and for the control of turnkey facilities within an MES environment.
Fully compliant with 21 CFR Part 11, GAMP 5, and ISA-88 (S88) requirements, this pre-qualified system is particularly well suited for biopharmaceutical manufacturing applications operating in a GMP environment.
PIERRE GUERIN is an OEM partner within the DeltaV™ Life Sciences OEM Program.
PIERRE GUERIN is a member of the Emerson DeltaV™ Life Sciences OEM Program.
This program structures the collaboration between Emerson and selected OEM partners in order to:
- Develop standardized DeltaV™ architectures
- Strengthen the technological consistency of solutions
- Improve system integration and maintainability
- Provide tailored support to the installed base
This partnership is part of a structured engineering approach designed to ensure technical continuity and long-term reliability for end-users.
“ Very thrilled to welcome Pierre Guerin as our newest member to the Emerson Global Life Science OEM Program! We had the privilege of hosting a fruitful kickoff meeting in Niort, France. During this session we discussed several joint automation and digitalization initiatives that will drive innovation and growth in the life science sector. ”
Main features
- Use of the PCSD library (Emerson standard objects)
- Process optimization through advanced functionalities: gravimetric control for precise dosing, Split-Range control up to 6 control actions
- Simple and intuitive user interface suitable for standalone units, multi-equipment installations, or full plant applications
- 21 CFR Part 11 compliant and developed in accordance with GAMP 5 guidelines
- Single-station or Client/Server architecture (distributed architecture)
- Audit Trail ensuring full traceability of modifications, events, and data within a single database
- Scalable platform with on-demand I/O expansion (all types of I/O, at any location and at any time)
- High adaptability (online expansion, security features, and redundancy)
Applications
Control of complex, multi-equipment processes within industrial environments dedicated to Life Sciences. This solution is particularly well suited for biopharmaceutical applications operating in a GMP environment.
