| Company
profile
CRONIMO was founded in 1963 by
an Austrian-Dutch family who, with effort and courage brought the
knowledge to design and construct Stainless Steel equipment, from
Europe to Argentina.
Today, CRONIMO designs, builds and assembles - in a 12,000 sqft
covered facility - equipment and machinery for the pharmaceutical,
chemical and food processing industry.
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Maintain the highest possible quality combined
with the most advanced manufacturing methods. |
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| Respect, apply and incorporate into our
products the most stringent and latest applicable norms related
to quality and performance (cGMP, 21CFR part 11, FPD, CE and Gamp
IV). |
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| Meet and exceed our customers' expectations
with modern products, constantly updated and improved; however
maintaining our widely recognized quality and reliability which
helped us to grow. Produce environmental friendly and operationally
safe equipment. |
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Train and support our representatives properly,
in many parts of the world so that they can assist, advise and
inform our present and future customers worldwide. |
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| Assure our customers worldwide a personalized
and focussed post-sales attention and service. |
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| Re-invest the benefits of gained experience
in the constant upgrading of all our resources in order to offer
the most advanced equipment possible. |
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| Develop and implement the best and most
effective export policies and practices in order to expand our
activities for the benefit of our company, its employees and vendors
and by doing so, taking advantage of an economy of scale, and
be able to offer the most competitive prices to our customer. |
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| Participate actively in the development of
our community by constantly upgrading the professional capabilities
of all our human resources. |
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| Besides its standard process equipment, CRONIMO
S.A. engages in the design and manufacturing of customized process
machinery and equipment. |
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Cronimo
has equipment to run tests to evaluate the performance of its machines
using
the customers own samples with written reports on results.
Depending on the equipment tested, reports are generated that confirm
their performance and trustworthiness
Equipment design utilities according to the client’s needs (Autocad
2000 “Inventor” and other 3D software)
"In Wall” design, charge and discharge systems, drums and
other accessories.
Equipment validation is, nowadays, an integrated part of the mandatory
methods of cGMP manufacturing in pharmaceutical equipment.
It is through the testing and systematic documentation of development
and production methods that the conduction of the process is achieved.
Our package includes:
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PQ Design
Qualification |
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IQ Installation
Qualification |
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OQ Operational Qualification
Test |
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FAT Factory Acceptance
Test |
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SAT Site Acceptance
test |
| And our support
for PQ (Performance Qualification) and equipment validation.
The modular concept enables the client to exactly fit its individual needs.
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