Development and implementation QMS according to ISO17025/9001 and GMP for pharmaceutical (contract-) laboratory. (certification laboratory/growing clientele)
Project Management, planning and documentation of "Cleaning validation project biochemical factory". (keep in compliance of factory for production after comments by authorities)
Restructuring laboratory supporting Department/management), redevelopment remuneration scales and function characteristics. (reorganization of Department to logical units, cost savings due to outflow staff)
Setting up Quality Agreement Life-cycle management program. (integrate GDP, GMP, Pharmacovigilance aspecten in de Business)
Registration Remediation project, including substantiation Gaps
Restructuring, harmonize and simplify quality & document management system for multiple factories, including clothes, cleaning en labeling regime.