Since it was founded, Sentinel has conducted business with the objective of:
• Providing clients with timely and reliable
responses to satisfy their needs.

• Understanding in advance the client’s expressed
and unexpressed needs

• Persevering in the continuous improvement
of its products

• Optimizing human resources
• Ensuring the growth of its organizational
structure, adequateness of procedures,
processes and flow of information

• Developing the company through
the improvement of results in terms of market
presence and profits to reinvest in research
and development.
Quality organizations
In fact, since 1998, Sentinel has had a certified quality management system and today it complies with the international regulations ISO 9001:2008 and ISO 13485:2003, the latter being specific to medical devices, including IVD.
The certificate obtained has been issued by the BSI (British Standards Institution), one of the most recognised certification bodies in the world; thus permitting Sentinel to meet the certification requirements at an international level.
Sentinel also promotes and sells its products
in the US, having registered its products
and manufacturing facility with the FDA.
Furthermore, in August 2006 it obtained certification ISO 13485:2003 CMDCAS standard, indispensable in order to sell products
on the Canadian market.
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Certifications
Sentinel Registered as a manufacturer of In-Vitro Diagnostic Medical Devices in the following countries:

- Italy, through the Italian Ministry of Health

- USA, listed as a registered establishment
in the FDA database
Sentinel is in possession of Certificates attesting
to compliance with the following standards:
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ISO 13485:2003
Quality Management Systems Requirements for regulatory purposes |
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Complying to 21 CFR 820
“Code of Federal Regulations“
FDA (U.S. Food and Drug Administration) |
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Moreover Sentinel is a Corporate Member of the IFCC (International Federation of Clinical Chemistry and Laboratory Medicine ) with a designated representative within the company. |


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Sentinel is accredited as a Validated Supplier by the IRMM (the European Commission Institute for Reference Materials and Measurements) and sponsors the research program of CIRME, the University of Milan's Centre of Metrological Traceability in Laboratory Medicine.
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