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Monday, 24 October, 2016


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Global Compliance Panel

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IEC 60601-1 Third Edition was released in late 2005. It is a new philosophy in standards for medical electrical devices to accommodate rapid advances in technology. This new philosophy has been difficult for test houses and compliance bodies to absorb and develop test strategies. Currently, the EU and Canada have announced May 31-June 1, 2012 as the date when the Second Edition will be withdrawn. Devices that will be released after that date must meet the requirements of the Third Edition. Manufacturers with products under development must start now to develop compliance strategies. The first step will be understanding the requirements of the new standard.
Title: Online Regulatory Compliance Training, FDA, Risk, and Compliance – GlobalCompliancePanel

GlobalCompliancePanel is an online knowledge fulfillment community portal. We are providing compliance training in various industries by expert speakers.

Category: Compliance - E-learning - Fda - Medical Devices - Compliance Training - Compliance Solutions - Regulatory Compliance - Compliance Management - Corporate Compliance

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