The task of evaluating and selecting a business system that will essentially run your business and help you meet U.S. Food and Drug Administration (FDA) requirements can be a daunting project. Having their ERP system validated gives the company and the FDA confidence and assurance that the company has control over their manufacturing processes and that they can quickly and easily identify product components by lot.

This white paper presents a guideline to help you select an ERP system for your FDA validation. Explore a five phase software acquisition life cycle model to help you accomplish these objectives as efficiently as possible.