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Langue du site : Français - English
Réf : 30323
Evènement :Medical Devices: EU Directives, CE marking, ISO Certification and the NEW Device Regulations coming to the EU

Date :Mercredi 11 Septembre 2019

Lieu :Palo Alto
2479 East Bayshore Road,
Suite 200
94303 Palo Alto, California, États-Unis

Type :Conférence & Séminaire - Audience Internationale

Accréditation :--


 

Informations

Editorial

This Medical device training will be discussing the requirements of the Medical Device Directives, their linkage to the EU Clinical Trial Directive and the requirements of CE Marking and ISO Certification on commercializing products.
 

Objectives

Upon completion of this course attendees will have a thorough knowledge of the requirements for developing and marketing Medical Devices in the European Union. The Directives are complex and the requirements differ somewhat by Member State. The content of this course is designed to simplify the understanding of all requirements and to provide attendees with the latest information regarding interpretation and enforcement of these regulations.
 

Program

This workshop will be of great value to Medical Device professionals and those involved in the registration of Medical Devices across the EU. It is primarily designed to benefit the following disciplines:

  • Clinical research and medical operations
  • Project Managers
  • Product Development personnel
  • Manufacturing personnel
  • Researchers managing Medical Device R&D and Development
  • Quality Assurance such as GMP, GCP Auditors
  • Regulatory affairs
  • Clinical trial supply personnel
  • CRO personnel
  • All personnel who need to understand the procedures and impact of placing Medical Devices on the Market in the EU (25 expanded countries)

 

Speakers

Robert J Russell
President, RJR Consulting, Inc
 

Lieu

Plan et itinéraire
Adresse de la conférence :
Palo Alto
2479 East Bayshore Road,
Suite 200
94303 Palo Alto
California, États-Unis
Tél : +1-888-717-2436
Plan et itinéraire

Renseignements

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Précisions

Medical Devices: EU Directives, CE marking, ISO Certification and the NEW Device Regulations coming to the EU Management
compliance training on medical device directives, directives for medical devices, training for medical device compliance, eu clinical trial directive compliance webinar, euctd compliance, ce marking for medical devices, requirements for ce marks, iso certification compliance for medical devices
Professionnels, This workshop will be of great value to Medical Device professionals and those involved in the registration of Medical Devices across the EU. It is primarily designed to benefit the following disciplines: Clinical research and medical operations Project Managers Product Development personnel Manufacturing personnel Researchers managing Medical Device R&D and Development Quality Assurance such as GMP, GCP Auditors Regulatory affairs Clinical trial supply personnel CRO personnel All personnel who need to understand the procedures and impact of placing Medical Devices on the Market in the EU (25 expanded countries)
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English

Divers

Pour plus d'informations sur Medical Devices: EU Directives, CE marking, ISO Certification and the NEW Device Regulations coming to the EU, veuillez contacter ComplianceOnline

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