In this post, Jama Software’s CEO discusses how living requirements can help reduce the risk of negative outcomes in the product development process.
In this blog post, we explain how to improve design control and risk management in medical device development by moving away from a document-based system.
Building and then bringing a medical device to market as quickly as possible—all while preserving acceptable levels of quality and regulatory compliance—requires adept medical device risk management. By minimizing potential risks such as mislabeling and software-related issues, medical device manufacturers make each product safer for the patients who will use them. All of these risks […]