Internal Quality Controls

Reliable IQC

control samples for laboratory techniques

Medical laboratories are required to verify the quality and reliability of the results of their analyzes, using internal quality control materials comparable to any patient sample. IBJB offers CQIs that meet the highest quality requirements. The CQI-IH are also independent, their results are known and guaranteed for any technique without restriction (filtration columns, plate, tube, microplate).
The advantages of a subscription
ICQ and dedicated services
Choose safety, efficiency and serenity.
Comfort
Wihen subscribing, you receive your IQC every 4 weeks. Flexible, the subscription is tacitly renewed at the end of the year but is not subject to any commitment of duration.
Constant quality
Each IQC meets the standards for DIV's. It is validated by an independent certifying body, and strictly controlled at each stage of its production.
Independance
Our IQC for IH do not come from the same manufacturer as the reagents and / or analyzers, they answer the professional and normative recommendations.
Our IQC
Application
fields
Immunohematology, Coombs test, HFM and genotyping, but also protocol and PLC validation, our IQCs are also a support in your accreditation procedures.
ABOD
blood grouping
Irregular
Antibodies
Searching
Direct
antiglobuline
test incl.
anti-complement
Protocol
validation
Fetal RHD
genotyping
Feto-maternal
hemorrage
quantification
Automata
checks
Recommandations

As a facilitator of your profession and a partner in your development,
we develop products that meet the constraints you must meet.

  • Giannoli JM, Szymanowicz A.
    Ann Biol Clin 2011 ; 69(4) : 489-98 doi :10.1684/abc.2011.0606
    Proposed recommendations for the practical use of internal quality controls (IQC) in a laboratory of medical biology:
    "The use of IQC independent from the device / reagent pair is the most recommended to ensure completely independent efficient internal control. "

  • NF EN ISO 15189 Norm
    Paragraph 5.6.2.2. "QC Materials" / extract
    «The use of independent third-party control materials should be considered instead of or in addition to control materials provided by the reagent or instrument manufacturer.»

  • Order of 15/05/18 laying down the conditions for carrying out BM erythrocyte IH tests
    Paragraph 2.4. "Direct examination with Antiglobulin" / extract
    «The demonstration of in vivo sensitization of red blood cells [...] requires the simultaneous and independent use of an anti-IgG antibody and an anti-C3d antibody as well as appropriate reactive controls.
    The analytical system is monitored using red blood cells previously sensitized in vitro with IgG- and red cells sensitized in vitro with complement.»

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