Milan Kucera is 25+ years of experienced in Information technology with major emphasis on information quality management, process improvement. Since 2014 I focus on Computerized System Validation, and QA/eCompliance with very good knowledge of GAMP practices and pharmaceutical regulatory e.g. cGMP, GDP, GCP, GLP, and EU Annexes (e.g. 11, 15), Good Documentation Practices, Risk Assessment, Change Management, Data Migration and System Lifecycle Documentation management for the Pharma industry,
