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4 Local Half-day Seminars

  • These seminars aim at promoting knowledge upgrade for medical device industry and enable them to interpret the actual rationale behind the new requirements, and to identifying practical implementation element for compliance with ISO13485:2016.

  • These 4 seminars will focus on the key changes between ISO13485:2003 and ISO13485:2016, actual rationale behind the requirements of ISO13485:2016, as well as the effective implementation of the new requirements in ISO13485:2016, where risk management is heavily involved.

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Risk Assessment for Procurement and Supplier Evaluation in Medical Device Life Cycle Seminar

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Risk Management during medical device realization and utilization cycle half -day seminar

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Seminar on Risk Management and Computer Software Validation in Manufacturing Process of Medical and Healthcare Device

Implementation Agent                                              Project Applicant                               Funding Agent

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"Any opinions, findings, conclusions or recommendations expressed in this material / any event organized under this Project do not reflect the views of the Government of the Hong Kong Special Administrative Region, Trade and Industry Department or the Vetting Committee for the SME Development Fund/Dedicated Fund on Branding, Upgrading and Domestic Sales (Organisation Support Programme)." 

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Funded by SME Development Fund

© 2017 Hong Kong Productivity Council. All Rights Reserved.

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