A key feature in the life sciences industry, IT compliance activity work in tandem with the quality management team. Good practices process is therefore is an essential feature for manufacturing, laboratory, research, and other systems from execution to automation. Every GxP qualified systems will undergo periodic quality assessment for compliance. Risk assessment forms the basis for compliance activities. Most of the organizations manage compliance along with quality, leading to a shift toward an internal, independent team that monitors compliance for all change management procedures. In fact, compliance management metrics is a key performance indicator during the change. This ensures the quality, control, and governance of the organizations’ IT environment.
- Industry Left Col
- Industry Right Col