Загрузка страницы
Все видеоНовые видеоПопулярные видеоКатегории видео

Medical Devices - ISO 14971 : Risk Management

This course provides the attendees with an overview of ISO 14971:2007 and implementation tips for an effective system for managing risk. We provide an overview using flow charts that shows each of the elements of a Risk Management system and how they fit together. This approach helps the participant understand the essential structure and the required elements.
For More Information Contact -

Organization: NetZealous BDA GlobalCompliancePanel
Website: http://www.globalcompliancepanel.com/
Email: support@globalcompliancepanel.com

Help us caption & translate this video!

http://amara.org/v/RLe3/

Видео Medical Devices - ISO 14971 : Risk Management канала GlobalCompliance Panel
Показать
Комментарии отсутствуют
Введите заголовок:

Введите адрес ссылки:

Введите адрес видео с YouTube:

Зарегистрируйтесь или войдите с
Информация о видео
18 июля 2016 г. 10:19:22
01:12:06
GlobalCompliance Panel
Теги
Правообладателям
Жалоба
Комментарии
Другие видео канала
Statistical Concepts of Process ValidationStatistical Concepts of Process ValidationRegulatory Documents Explained - DHF, DMR, DHR and TFRegulatory Documents Explained - DHF, DMR, DHR and TFMedical Devices in Hospital Networks: Mitigating Risk in 2016Medical Devices in Hospital Networks: Mitigating Risk in 2016Risk management for medical devices and ISO 14971 - Online introductory courseRisk management for medical devices and ISO 14971 - Online introductory courseA Risk-Based Approach to QMS Ahead of ISO 13485 ChangesA Risk-Based Approach to QMS Ahead of ISO 13485 ChangesSoftware as a Medical Device Classification Rule 11 (EU MDR 2017/745)Software as a Medical Device Classification Rule 11 (EU MDR 2017/745)How to Simplify Your Compliance with the New ISO 13485:2016How to Simplify Your Compliance with the New ISO 13485:2016Harvard i-lab | Understanding Medical Device DevelopmentHarvard i-lab | Understanding Medical Device DevelopmentThe 5 most relevant changes the Medical Device Regulation MDR introduces, that you must knowThe 5 most relevant changes the Medical Device Regulation MDR introduces, that you must knowHow to get ISO 13485 certified? (Quality Management System)How to get ISO 13485 certified? (Quality Management System)Best ISO 13485:2016 Starter Video [For Medical Devices]Best ISO 13485:2016 Starter Video [For Medical Devices]Design Controls - Requirements for Medical Device DevelopersDesign Controls - Requirements for Medical Device DevelopersElectrical Safety Testing For Medical DevicesElectrical Safety Testing For Medical DevicesISO 9001 IN A NUTSHELL | How it Works and How it Can Work For YouISO 9001 IN A NUTSHELL | How it Works and How it Can Work For YouWhat are the changes to ISO 14971 2019? (REPLAY) #medicaldeviceWhat are the changes to ISO 14971 2019? (REPLAY) #medicaldeviceComplaint Handling in Compliance with FDA and ISO RegulationsComplaint Handling in Compliance with FDA and ISO RegulationsSupplier Evaluation & Assessment How to Meet FDA QSR & ISO 13485 RequirementsSupplier Evaluation & Assessment How to Meet FDA QSR & ISO 13485 RequirementsHow to Categorize a Medical Device per ISO 10993-1How to Categorize a Medical Device per ISO 10993-1Evolution of ISO 13485:2016 and ISO 9001:2015 standardsEvolution of ISO 13485:2016 and ISO 9001:2015 standardsUnderstanding Attribute Acceptance Sampling including Z1 4 and c=0 PlansUnderstanding Attribute Acceptance Sampling including Z1 4 and c=0 Plans
Статистика портала
Яндекс.Метрика
© 2008-2024 «Информационно-развлекательный портал города Верхняя Салда»
| Карта портала | Реклама | Контакты | Сообщить об ошибке | Соглашения
salda.ws salda.ws@mail.ru
Сейчас на сайте: 512 Статистика портала