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S D AQUA FINE design and supply Mobile and Fixed CIP &
SIP Units for sanitization and sterilization.
The units are custom made, modular, skid either automatic or
semi-automatic models as per the requirement for cleaning and
sterilization.
CIP System
CIP Unit:
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CIP Tank/Tanks, Jacketed/Non-Jacketed
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Supply Pump/Return Pump
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Heater as required
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Dosing Tanks/Pumps
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Inter-connected Pipings/Valves/Instrumentation
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Automation System/Control Panel
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SS Skid/SS Platform
Mobile CIP Unit:
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Pure Steam Header with PI, TI & Safety Valve
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Condensate Header with sterile steam trap unit and Temp.
Sensor
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PLC Control Panel with Time/Temperature control program,
printer, alarm etc. as required
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SS Mobile Stand with PU Castors
Specifications:
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Sanitary Design to meet all CGMP criteria
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Contact parts : SS 316L, Mirror polished & EP
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All Non – Contact parts : SS 304 Matte finish
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Orbital Tube welding
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Automation as per MCA & USFDA 21 CFR Part 11
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Built to custom requirement
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100% Drainability
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GMP documentation like DQ, FAT, IQ, OQ & PQ Protocols
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Site Installation & Commissioning
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Documented Output of cleaning & sterilization cycles
Applications:
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Pharmaceutical
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Biotechnology
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Food
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Beverage
Construction features:
These plants are manufactured according to CGMP std. All
equipments and plants are manufactured using sanitary AISI 316 L
Stainless steel electro polished tubes and fittings with surface
finish of Ra < 0.4 um. All piping and fittings are welded using
latest Orbital welding machines.
Automation:
S D AQUA FINE plants are PLC based fully automatic and have
necessary safety interlocks, data logging facility and intuitive
software for smart control and monitoring of the system. The
pumps can be provided with variable frequency drives (VFD) on
request. Various instruments like flow, pressure transmitters,
conductivity, pH and ORP analyzers continuously monitor the
plant performance and the data is logged for easy review and
study..
Documentation:
S D AQUA FINE’s CIP / SIP System is provided with documentation
backed with necessary test and calibration certificates with
full NABL traceability. For pharmaceutical and biotechnology
industry. the documentation is done to ensure proper regulatory
compliance. (DQ, FAT, IQ, OQ, and PQ).
The documentation package is well designed and organized to
provide validated information on the Project life cycle from
design stage to site to acceptance test. Our dedicated
Validation Team provides a comprehensive Validation Support to
the customer including Validation Protocol preparation, Site
Tests activities, Instrumentation Calibration and Validation
Reports organization.
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