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Webinar – Post Market Surveillance secondo MDR
by admin|3 May 2021|Company News
Webinar  - Giovedì 13.05.2021 Ore 10:00 - 11:00 Post Market Surveillance secondo MDR
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ISO 20417:2021 Medical devices – Information to be supplied by the manufacturer
by admin|27 April 2021|Medical
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Webinar – Biocidi e PMC …. Cosa c’è da sapere
by admin|27 April 2021|Company News
Webinar  - Mercoledì 05.05.2021 Ore 10:00 - 13:00 Biocidi e PMC ... Cosa c'è da...
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Produzione biologica ed etichettatura: Il regolamento 2018/848
by admin|20 April 2021|Food
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Free Webinar – La valutazione biologica: cosa cambia con l’MDR e i nuovi standard di riferimento
by admin|19 April 2021|Company News
Webinar gratuito  - Giovedì 29.04.2021 Ore 10:00 - 11:00 La valutazione biologica: cosa cambia con...
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Application of transitional provisions for certification of class D in vitro diagnostic medical devices according to Regulation 2017/746
by admin|13 April 2021|Medical
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Free Webinar – Comprendere gli articoli: cosa c’è a monte della notifica SCIP
by admin|13 April 2021|Company News
Webinar gratuito  - Giovedì 22.04.2021 Ore 11:00 - 12:00 Comprendere gli articoli: cosa c'è a...
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REACH: a new version in 2022?
by admin|6 April 2021|Chemical
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Free Webinar – ISO 13485: Dispositivi medici – Sistema di gestione per la qualità – Requisiti per scopi regolamentari
by admin|31 March 2021|Company News
Webinar gratuito  - Giovedì 14.04.2021 Ore 10:00 - 11:00 Questo Webinar da una introduzione agli...
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Medical devices: EU regulations for MDR and IVDR (Northern Ireland)
by admin|30 March 2021|Medical
[vc_acf field_group="1287" field_from_1287="field_5a155fb5628a4"] [vc_acf field_group="1287" show_label="yes" field_from_1287="field_5a1538a612368"][vc_acf field_group="1287" show_label="yes" field_from_1287="field_5a15385612367"][vc_acf field_group="1287" show_label="yes" field_from_1287="field_5a1539cf1236a"] [latest_post type="minimal"...
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