Pharmacometricians perform complex analyses in a highly regulated and dynamic environment under increasing time pressures from internal and external stakeholders. A consistent MIDD workflow incorporating principles and concepts spanning the model development continuum from planning to reporting can help to ensure quality and efficiency in our analyses; thereby, allowing more resources to be dedicated to innovative models and approaches. This presentation will cover key points for consideration on pharmacometrics workflow from the ISoP Standards and Best Practices Workflow Sub-Committee.
