How Aras PLM Improves Risk Management In Medical Device Development

Product recalls are often consequences of quality failures. That is why quality management is essential to making any product. Medical device development is all about mitigating risk, and quality assurance and control play a vital role. But without a connection between enterprise Quality Management Systems, ERP, CAD, and Product Data Management Systems, information is not always communicated clearly throughout the lifecycle.

Miscommunication often leads to mistakes, component failures, and, ultimately, a product recall. Avoid this scenario and detect quality issues before they become a problem. By connecting all information on products, components, and documents, you can capture all revisions and changes made and ensure that all changes are communicated to everyone involved in the product development lifecycle.