Simplify Compliance and Reduce the Cost of Quality
Quality issues can arise throughout the product lifecycle. Accelerating product development, quality, and CAPA processes, and the resolution of quality or design issues with product-centric cloud QMS, ensures fast delivery of safe and compliant products.
For medical device companies, FDA or quality system noncompliance issues can determine the success or failure of a product launch and, sometimes, the company itself. Centralizing the creation, review, and approval of product and quality information reduces audit risks, ensures regulatory compliance, and drives continuous improvement.