Process Solutions
Innovative and sustainable process solutions for pharma, biopharma and biotech industries
Pharma and biopharma applications demand that high purity and process technologies evolve to keep pace with a changing drug manufacturing landscape.
Our experienced design, engineering, and automation teams have client-side experience and work closely with you to customise a sustainable solution that optimises your processes and delivers sterile integrity.
DESIGN & QUALITY COMPLIANCE STANDARDS
Vessel Design
- ASME BPE 2016 for vessel and piping manufacturing
- ASME Section VIII, Div. 1 for pressure vessel manufacturing
Process Design
- US FDA 21 CFR 177.2600 for gaskets and O-rings
- ASME BPE 2016 for vessel and piping manufacturing
Automation Design
- US FDA 21 CFR Parts 11 for Electronic records and electronic signatures.
- GAMP for Validation of Automated System
- GAMP 5 for a risk-based approach to compliant GxP Computerized Systems
Electrical Design
- IEC 60529 standards for panel enclosure protection
- EN/IEC-60204 and UL 508 for electrical work
- CE Marking Compliance Testing and Certification
Our range of process solutions
Process
Manufacturing Vessels for sterile pharma, injectables
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Process
Manufacturing vessels for biopharma
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Process
Manufacturing Vessels for biotech
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Process
CIP/SIP System
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CIP/SIP System
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Bio Kill System
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Bio Kill System
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Process
Heat Exchanger
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Heat Exchanger
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Process
Process Piping
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Process Piping
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Process Automation
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