Industries that must adhere to FDA regulations—such as food and beverage manufacturers, pharmaceuticals, medical devices, and others—are legally required to validate any software that could impact product quality, safety, or effectiveness. And while the FDA provides guidelines regarding software validation, it does not tell companies exactly how to do it.
If your organization belongs to an FDA-regulated industry, you can learn how to make an informed decision about how to handle your company’s FDA software validation compliance needs, including:
- Eight crucial questions for your leadership to consider that can help you decide whether or not you have the internal resources to successfully complete all compliance activities
- The differences between computer system validation and computer software assurance, and why both of these are important
- How an integrated, configurable ERP can help your company manage FDA requirements, product recalls, and other key business needs
Download today and learn how to take the next steps in FDA compliance.