Virus Genome Detection - Respiratory Virus Panel 1 for Multiplex Tests (431)

4 samples of 1.5 ml
Proprietà campione:
Lyophilised cell culture lysates


Termine di registrazione:

Spedizione del campione:

Data di chiusura:

June (4) Nov. (6)
12.04.2024 06.09.2024
11.06.2024 05.11.2024
28.06.2024 22.11.2024
Informazioni sulla spedizione:
Shipping at ambient temperature
Polymerase chain reaction (PCR) and other nucleic acid amplification techniques (NAT) for simultaneous qualitative detection of respiratory adeno, boca, corona, entero, human metapneumo, human rhino, influenza A and B viruses incl. avian influenza A viruses, parecho, parainfluenza, respiratory syncytial viruses (groups A and B) and SARS-CoV-2 (inactivated), respectively. This program will be completed with currently circulating virus variants. Some of the samples can contain chemically inactivated avian influenza A viruses.
Validità del certificato:
12 months
Avviso di sicurezza:
Process as patient sample material. The participating laboratory must be authorized to perform direct and/or indirect detection of pathogens.
Informazioni aggiuntive:
The requirements of the RiliBÄK (Guidelines of the German Medical Association on quality assurance in medical laboratory testing / Bundesärztekammer) will be considered for the detection of the above-mentioned pathogens. This EQA scheme will contain each of the above-mentioned pathogens at least once a year. It is recommended to participate at both EQA scheme terms. Please note: Only results of multiplex tests will be accepted for EQA scheme 431 This multiplex EQA scheme is not suitable for (i) singleplex PCRs, (ii) tests for antigen detection, (iii) testing of sensitivity and (iv) typing. For this purpose, we refer to the INSTAND EQA schemes for the corresponding viruses. Note for laboratories from non-EU countries: The shipment of sample materials for participation in this EQA scheme is subject to a release by the Federal Office of Economic Affairs and Export Control according to the EU Dual-Use Regulation (VO (EU) 2021/821) for sample recipients in non-EU countries. INSTAND e.V. can only process EQA scheme orders from non-EU countries if the ordering laboratories provide a completed end-use certificate, company profile including contact details (e.g. excerpt from website) and, if applicable, an import permit! Failure to provide completed documents by the ordering deadline will unfortunately lead to the cancellation of your registration.
Esperto EQAS:

Dr. rer. nat. Rolf Kaiser, Dipl.-Biol.

Institut für Virologie

Universität und Universitätsklinikum zu Köln

Fürst-Pückler-Straße 56

50935 Köln


+49 221 478-85808


Dr. rer. nat. Martin Kammel

Institut für Qualitätssicherung in der Virusdiagnostik - IQVD


Potsdamer Chaussee 80

14129 Berlin


+49 30 8105 4300