Quality control

QUALITY CONTROL Product Line

Quality Control is an Essential Tool for Monitoring Analytical Performance

Quality Controls are standardized materials designed to independently evaluate the overall performance of the analytical process. Used periodically, they allow:

  1. Verify the accuracy and precision of results across multiple analytical sessions.
  2. Identify systematic errors or random errors related to variations in batch, reagents, protocols, instrumentation, or operators.
  3. Monitor the consistency of results against international standards, reducing the risk of undetected anomalies.

Virological Serology

Chemistry and Immunometry

Hematology and Coagulation

Flow Cytometry

Molecular biology

Drugs of Abuse and Toxicology

NGS Reference Material

Additional QC

INTERQC Management Software

The use of quality controls ensures reliable results that comply with quality standards and represents a fundamental requirement for accredited and certified laboratories.

The main characteristics of Quality Control are:

  1. Standardized Composition

  • Similar to real samples: the control material must mimic the chemical, physical, or biological properties of clinical samples (Patient Human-like)

  • Produced with highly purified components to ensure consistency between batches.

  1. Stability

  • It must maintain its characteristics over time, even during transport and storage in various environmental conditions.

  • Ensures long shelf life for repeated and reliable use.

  1. Representativeness

  • It must cover a wide range of analytical values (low, intermediate, high) to simulate various clinical conditions.

  • Essential for detecting deviations in qualitative and quantitative tests.

  1. Traceability and Recognitions

  • Certifications compliant with international standards (ISO 15189, ISO 13485 ISO 17511, CAP, CLIA).

  • Accompanied by comprehensive documentation, including information on traceability, stability, and validation.

  1. Precision and Accuracy

  • Designed to monitor the entire analytical process: from sample preparation to result generation.

  • Allows detection of systematic errors (e.g., batch variations) and random errors (e.g., technical operations).

  1. Applicability and Compatibility

  • Suitable for various instruments, reagents, and protocols used in laboratories.

  • Compatible with major diagnostic techniques

  1. Support for Regulatory Compliance

Its use is required by Good Laboratory Practice (GLP) regulations and accreditation standards for diagnostic laboratories.

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Quality control

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