Process Automation
Design to Delivery: Process automation life cycle at Praj Hipurity Systems Limited
In Pharma, Biotech & Vaccines, Process Automation is a key driver for ensuring the success of production batches. The need is to meet up to-
- Regulatory needs
- Documentation needs
- Process needs
- Repeatability
- Functional Design
- Hardware Design
- Software Design
Instruments
- Process parameters
- Process end Connection
- Material Of construction
- Range
- Accuracy
- Pressure ratings
- Temperature ratings
- Multiplicity of outputs
- Signal communications
- Hygienic mounting
- Construction
- Readability
- Calibration
- Spares (needs & availability)
- Lead time
- Price
Supply Chain Management (SCM)
Development & Quality Control
- Phase 1 standardization
- Phase 2 simplification
- Phase 3 specialization
- Function Design Manual (FDM)
- Hardware Design Manual (HDM)
- Software Design Manual (SDM)
These help to construct Faceplates in concurrence with our process team ( with process, design expertise over many years in different roles of researchers, designers as well as users).
It is also important to sequence the design process from the finalization of the specification to FAT/SAT.
Stage wise inspection of the program including a robust bench testing process is the key to success. It is important for Praj Hipurity Systems Limited team and client to arrive upon a common consensus very early in the project and freeze critical aspects (including and not limited to report formats, mimic screens, sequences, alarms, audit/trend reports, electronic signatures, data backup and restore, etc.)
Design To Delivery: System Architecture

Design To Delivery: Guiding Principle

Design To Delivery: Praj Hipurity Systems Limited deliverable towards GAMP 5 Documentation

Design To Delivery: Development & Inspections

Design To Delivery: Commissioning & Support
