13-14 Sept 2017 : Medical Device Manufacturing Process Validation, KL

AMMI organised the training on Medical Device Process Validation Training at Dorsett Grand Subang (13-14 Sept 2017). Thirty (30) participants from eleven (11) companies attended the training  which was conducted by industry expert, Mr Gobu Devarajan.  The course provided regulatory/quality systems professionals, manufacturing engineers, and process development engineers with the knowledge and skills needed to comply with the process validation requirements of the FDA’s Quality System Regulation, ISO 13485 and the GHTF Validation guidance N99-10 while offering information on how to implement an effective validation program.
Class in Session…
Participants were divided into groups during the Workshop Session.

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