Updated August 13, 2026

IMQ is a conformity assessment body based in Italy, identified as notified body NB 0051. NANDO lists it as currently designated under the EU Medical Devices Regulation (MDR) and the In Vitro Diagnostic Medical Devices Regulation (IVDR). Its detailed NANDO scope shows the device categories and conformity assessment activities covered by that designation.

1 Review

2.0 Very bad · 1 review
Read all reviews
Overall experience
2.0
Well-organized / responsive
2.0
Regulatory pragmatism
2.0
Technical competence
3.0
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March 01, 2022

Review by company with 1-9 people

QMS audit done
Techdoc audit done
Overall experience
Well-organized / responsive
Regulatory pragmatism
Technical competence
Wait time before QMS audit
18 Months
Wait time before Techdoc audit
18 Months
Wait time before QMS certificate
1 Month
Wait time before Techdoc certificate
18 Months
Approx. cost (EUR)
Not specified
Too long time to receive any response. Some NC without any sense. More than 6 months to checks their forms and start to review our TF

Additional Comments (Duration/Cost): More than 20.000€

No, I would not choose this notified body again.

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