Erick Gaussens, ProductLife Group’s chief scientific officer, reports on a recent pharmaceutical roundtable which examined why streamlining data management between regulatory and manufacturing needs is a pressing concern for manufacturers.
Data
Maintaining separate information systems to manage product data no longer serves life sciences firms. Compliance, cost-efficiency and improved agility depend on building closer links between enterprise resource planning (ERP) and regulatory information management (RIM), and reducing the number of separate instances of the same information being captured, stored and updated.
On the panel were: