Laboratory medicine is impacted by constant transformations that affect the products offered. The demands are growing, both internally and externally.

Externally there are the legal and regulatory requirements, the new expectations and needs of clients (requesting clinical staff, patients and their families, paying sources and researchers), the recommendations and guidelines of scientific societies, technological innovations, the pressure of competition and suppliers with a variety of new products.

Internally, laboratory managers and their teams need to demonstrate increasing levels of technical excellence on a daily basis to ensure the reliability of their results. However, with ever short delivery times, expanded menu of tests offered and lower prices to maintain their competitiveness.

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Among these routines, the following stand out:

Pre-analytical phase

It involves the qualification of samples that depend on the preparation of the patient, the collection performed, the packaging of the samples and the transport.

Analytical phase

It includes qualified products, materials and services, control and processing of biological material and teams performing tests.

Post-analytical phase

There is a relevant clinical laboratory correlation and the exact clinical interpretation of the results.
Há a relevante correlação clínico laboratorial e a exata interpretação clínica dos resultados.

For this reason, even in the face of a great development of analytical processes, including methodological evolution and automation, publications still point to a chance of errors occurring within the analytical phase.

The rapid evolution of processes has also required better training of professionals and the adoption of effective management tools by laboratories, to ensure the quality of results.

International standardization institutes have described guidelines in this regard, accreditation bodies have encouraged the adoption of these guidelines and, in some cases, government agencies have been expanding the basic requirements for the operation of laboratories and their suppliers.

Ensaio de Proficiência (EP)

Periodic external evaluation to
ensure result accuracy.

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Continuous monitoring to identify
and correct routine errors.

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Comparative management of indicators for
precise strategic decisions.

strains of reference

NCTC®️ culture collection with
technical equivalence to ATCC®️.
(according to wdcm.org)

Materiais de Referência Certificados (MRC)

Traceability and accuracy aligned with
international standards.

Calibração de Instrumentos (CA)

Instrument verification to prevent
measurement errors.

In Vitro Diagnostic

Partnerships to promote quality and safety
in vitro diagnostic products.

Distance Learning

Training programs to enhance
laboratory practices.

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HAVE AN ENVIRONMENT WITH ANALYSIS OF EXCELLENCE

Controllab offers complete solutions for quality and assertiveness of results. These solutions facilitate recognition for accreditation processes and regulatory bodies.

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