| AMMI-Medsociate organised its Industry Expert Series Training Course on Medical Device Manufacturing Process Validation at E&O Hotel Penang from 1-2 June 2016. The 2-day course was designed to
provide 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 programme. |
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