S D AQUA FINE RO-EDI Plants are used for Generation of
High Purity water for pharmaceutical, Biotechnology, Cosmetic
and Food & Beverages Industry. Many years of experience and
continuous development has led to all our plants being very user
friendly and robust. The plants are built using world class
equipment’s and are engineered with highest care to ensure peak
performance throughout its life span.
RO EDI Plant
Important features of S D AQUA FINE RO-EDI Plants:
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Pre-engineered packaged plants and custom built plants as
per URL
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The plants can be either chemical or hot water Sanitisable
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Complete design with low footprint
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Plants manufactured as per ASME, BPE and ISPE Guidelines.
Advantages of RO EDI Plants:
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 RO EDI 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 RO EDI plant 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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