�ݺ�ߣshows by User: StefanoBolletta

�ݺ�ߣshows by User: StefanoBolletta / http://www.slideshare.net/images/logo.gif �ݺ�ߣshows by User: StefanoBolletta / Thu, 18 Jan 2018 09:01:59 GMT �ݺ�ߣShare feed for �ݺ�ߣshows by User: StefanoBolletta Tuv sud-ivdr-infosheet - EU’s In Vitro Diagnostic Medical Device Regulation /slideshow/tuv-sudivdrinfosheet-eus-in-vitro-diagnostic-medical-device-regulation/86338334 tuv-sud-ivdr-infosheet-180118090159
EU’s In Vitro Diagnostic Medical Device Regulation A quick guide to the new IVDR. The EU’s in vitro diagnostic medical device regulation Manufacturers of in vitro diagnostic medical devices seeking market access to the European Union (EU) will soon face major changes in the EU’s decades-old regulatory framework. The EU’s In vitro diagnostic medical device regulation (IVDR) was officially published on 5 May 2017 and came into force on 26 May 2017. The IVDR will replace the EU’s current directive on in vitro diagnostic medical devices (98/79/EC).]]>
EU’s In Vitro Diagnostic Medical Device Regulation A quick guide to the new IVDR. The EU’s in vitro diagnostic medical device regulation Manufacturers of in vitro diagnostic medical devices seeking market access to the European Union (EU) will soon face major changes in the EU’s decades-old regulatory framework. The EU’s In vitro diagnostic medical device regulation (IVDR) was officially published on 5 May 2017 and came into force on 26 May 2017. The IVDR will replace the EU’s current directive on in vitro diagnostic medical devices (98/79/EC).]]> Thu, 18 Jan 2018 09:01:59 GMT /slideshow/tuv-sudivdrinfosheet-eus-in-vitro-diagnostic-medical-device-regulation/86338334 StefanoBolletta@slideshare.net(StefanoBolletta) Tuv sud-ivdr-infosheet - EU’s In Vitro Diagnostic Medical Device Regulation StefanoBolletta EU’s In Vitro Diagnostic Medical Device Regulation A quick guide to the new IVDR. The EU’s in vitro diagnostic medical device regulation Manufacturers of in vitro diagnostic medical devices seeking market access to the European Union (EU) will soon face major changes in the EU’s decades-old regulatory framework. The EU’s In vitro diagnostic medical device regulation (IVDR) was officially published on 5 May 2017 and came into force on 26 May 2017. The IVDR will replace the EU’s current directive on in vitro diagnostic medical devices (98/79/EC). <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/tuv-sud-ivdr-infosheet-180118090159-thumbnail.jpg?width=120&height=120&fit=bounds" /> EU’s In Vitro Diagnostic Medical Device Regulation A quick guide to the new IVDR. The EU’s in vitro diagnostic medical device regulation Manufacturers of in vitro diagnostic medical devices seeking market access to the European Union (EU) will soon face major changes in the EU’s decades-old regulatory framework. The EU’s In vitro diagnostic medical device regulation (IVDR) was officially published on 5 May 2017 and came into force on 26 May 2017. The IVDR will replace the EU’s current directive on in vitro diagnostic medical devices (98/79/EC).

Tuv sud-ivdr-infosheet - EU’s In Vitro Diagnostic Medical Device Regulation from Stefano Bolletta

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0 Tuv sud-biological-evaluation-of-medical-devices-it /slideshow/tuv-sudbiologicalevaluationofmedicaldevicesit/79797943 tuv-sud-biological-evaluation-of-medical-devices-it-170915071344
Valutazione biologica dei Dispositivi Medici Garantire la sicurezza dei Dispostivi Medici.]]>
Valutazione biologica dei Dispositivi Medici Garantire la sicurezza dei Dispostivi Medici.]]> Fri, 15 Sep 2017 07:13:44 GMT /slideshow/tuv-sudbiologicalevaluationofmedicaldevicesit/79797943 StefanoBolletta@slideshare.net(StefanoBolletta) Tuv sud-biological-evaluation-of-medical-devices-it StefanoBolletta Valutazione biologica dei Dispositivi Medici Garantire la sicurezza dei Dispostivi Medici. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/tuv-sud-biological-evaluation-of-medical-devices-it-170915071344-thumbnail.jpg?width=120&height=120&fit=bounds" /> Valutazione biologica dei Dispositivi Medici Garantire la sicurezza dei Dispostivi Medici.

Tuv sud-biological-evaluation-of-medical-devices-it from Stefano Bolletta

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0 The EU’s Medical Device Regulation /slideshow/the-eus-medical-device-regulation/79056521 tuv-sud-mdr-factsheet-170822144037
The EU’s medical device regulation Medical device manufacturers seeking market access to the European Union (EU) will soon face major changes in the EU’s decades-old regulatory framework. The EU’s Medical Device Regulation (MDR) was officially published on 5 May 2017 and came into force on 25 May 2017. The MDR will replace the EU’s current Medical Device Directive (93/42/EEC) and the EU’s Directive on active implantable medical devices (90/385/EEC).]]>
The EU’s medical device regulation Medical device manufacturers seeking market access to the European Union (EU) will soon face major changes in the EU’s decades-old regulatory framework. The EU’s Medical Device Regulation (MDR) was officially published on 5 May 2017 and came into force on 25 May 2017. The MDR will replace the EU’s current Medical Device Directive (93/42/EEC) and the EU’s Directive on active implantable medical devices (90/385/EEC).]]> Tue, 22 Aug 2017 14:40:37 GMT /slideshow/the-eus-medical-device-regulation/79056521 StefanoBolletta@slideshare.net(StefanoBolletta) The EU’s Medical Device Regulation StefanoBolletta The EU’s medical device regulation Medical device manufacturers seeking market access to the European Union (EU) will soon face major changes in the EU’s decades-old regulatory framework. The EU’s Medical Device Regulation (MDR) was officially published on 5 May 2017 and came into force on 25 May 2017. The MDR will replace the EU’s current Medical Device Directive (93/42/EEC) and the EU’s Directive on active implantable medical devices (90/385/EEC). <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/tuv-sud-mdr-factsheet-170822144037-thumbnail.jpg?width=120&height=120&fit=bounds" /> The EU’s medical device regulation Medical device manufacturers seeking market access to the European Union (EU) will soon face major changes in the EU’s decades-old regulatory framework. The EU’s Medical Device Regulation (MDR) was officially published on 5 May 2017 and came into force on 25 May 2017. The MDR will replace the EU’s current Medical Device Directive (93/42/EEC) and the EU’s Directive on active implantable medical devices (90/385/EEC).

The EU’s Medical Device Regulation from Stefano Bolletta

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0 Cardiovascular medical devices /slideshow/cardiovascular-medical-devices/78030130 cardiovascularmedicaldevices-170719072632
Cardiovascular Medical Devices Assessing the Safety of Cardiovascular Medical Devices.]]>
Cardiovascular Medical Devices Assessing the Safety of Cardiovascular Medical Devices.]]> Wed, 19 Jul 2017 07:26:32 GMT /slideshow/cardiovascular-medical-devices/78030130 StefanoBolletta@slideshare.net(StefanoBolletta) Cardiovascular medical devices StefanoBolletta Cardiovascular Medical Devices Assessing the Safety of Cardiovascular Medical Devices. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/cardiovascularmedicaldevices-170719072632-thumbnail.jpg?width=120&height=120&fit=bounds" /> Cardiovascular Medical Devices Assessing the Safety of Cardiovascular Medical Devices.

Cardiovascular medical devices from Stefano Bolletta

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0 TÜV Examination Institute /slideshow/tv-examination-institute/74440004 flyerpjm-170405101346
La certificazione del Project Manager Project manager è una delle figure più diffuse nel mercato nazionale ed internazionale del lavoro. Con la pubblicazione della norma UNI 11648:2016, il legislatore ha definito in maniera chiara quali sono le conoscenze, competenze ed abilità che un Project Manager, o responsabile di progetto, deve possedere per gestire i progetti affidatigli. La certificazione del personale, rilasciata da un ente terzo ed imparziale, è un efficace strumento per valorizzare le proprie competenze e per il riconoscimento e la spendibilità della propria professione nel libero mercato. A tale scopo TÜV Italia ha sviluppato uno schema per la certificazione di questa importante figura professionale in accordo alle norme UNI 11648:2016, UNI ISO 21500:2013 e UNI CEI EN ISO/IEC 17024:2012.]]>
La certificazione del Project Manager Project manager è una delle figure più diffuse nel mercato nazionale ed internazionale del lavoro. Con la pubblicazione della norma UNI 11648:2016, il legislatore ha definito in maniera chiara quali sono le conoscenze, competenze ed abilità che un Project Manager, o responsabile di progetto, deve possedere per gestire i progetti affidatigli. La certificazione del personale, rilasciata da un ente terzo ed imparziale, è un efficace strumento per valorizzare le proprie competenze e per il riconoscimento e la spendibilità della propria professione nel libero mercato. A tale scopo TÜV Italia ha sviluppato uno schema per la certificazione di questa importante figura professionale in accordo alle norme UNI 11648:2016, UNI ISO 21500:2013 e UNI CEI EN ISO/IEC 17024:2012.]]> Wed, 05 Apr 2017 10:13:46 GMT /slideshow/tv-examination-institute/74440004 StefanoBolletta@slideshare.net(StefanoBolletta) TÜV Examination Institute StefanoBolletta La certificazione del Project Manager Project manager è una delle figure più diffuse nel mercato nazionale ed internazionale del lavoro. Con la pubblicazione della norma UNI 11648:2016, il legislatore ha definito in maniera chiara quali sono le conoscenze, competenze ed abilità che un Project Manager, o responsabile di progetto, deve possedere per gestire i progetti affidatigli. La certificazione del personale, rilasciata da un ente terzo ed imparziale, è un efficace strumento per valorizzare le proprie competenze e per il riconoscimento e la spendibilità della propria professione nel libero mercato. A tale scopo TÜV Italia ha sviluppato uno schema per la certificazione di questa importante figura professionale in accordo alle norme UNI 11648:2016, UNI ISO 21500:2013 e UNI CEI EN ISO/IEC 17024:2012. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/flyerpjm-170405101346-thumbnail.jpg?width=120&height=120&fit=bounds" /> La certificazione del Project Manager Project manager è una delle figure più diffuse nel mercato nazionale ed internazionale del lavoro. Con la pubblicazione della norma UNI 11648:2016, il legislatore ha definito in maniera chiara quali sono le conoscenze, competenze ed abilità che un Project Manager, o responsabile di progetto, deve possedere per gestire i progetti affidatigli. La certificazione del personale, rilasciata da un ente terzo ed imparziale, è un efficace strumento per valorizzare le proprie competenze e per il riconoscimento e la spendibilità della propria professione nel libero mercato. A tale scopo TÜV Italia ha sviluppato uno schema per la certificazione di questa importante figura professionale in accordo alle norme UNI 11648:2016, UNI ISO 21500:2013 e UNI CEI EN ISO/IEC 17024:2012.

Tテ弖 Examination Institute from Stefano Bolletta

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0 TÜV Italia Journal n°11 /slideshow/tv-italia-journal-n11/73958503 tj-11-170330102846
Innovazione: l'era digitale trasforma il quotidiano]]>
Innovazione: l'era digitale trasforma il quotidiano]]> Thu, 30 Mar 2017 10:28:45 GMT /slideshow/tv-italia-journal-n11/73958503 StefanoBolletta@slideshare.net(StefanoBolletta) TÜV Italia Journal n°11 StefanoBolletta Innovazione: l'era digitale trasforma il quotidiano <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/tj-11-170330102846-thumbnail.jpg?width=120&height=120&fit=bounds" /> Innovazione: l'era digitale trasforma il quotidiano

Tテ弖 Italia Journal nツー11 from Stefano Bolletta

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0 https://public.slidesharecdn.com/v2/images/profile-picture.png https://cdn.slidesharecdn.com/ss_thumbnails/tuv-sud-ivdr-infosheet-180118090159-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/tuv-sudivdrinfosheet-eus-in-vitro-diagnostic-medical-device-regulation/86338334 Tuv sud-ivdr-infosheet... https://cdn.slidesharecdn.com/ss_thumbnails/tuv-sud-biological-evaluation-of-medical-devices-it-170915071344-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/tuv-sudbiologicalevaluationofmedicaldevicesit/79797943 Tuv sud-biological-eva... https://cdn.slidesharecdn.com/ss_thumbnails/tuv-sud-mdr-factsheet-170822144037-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/the-eus-medical-device-regulation/79056521 The EU’s Medical Devic...