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.