Why is Quality Assurance and Quality Control Important in Medical Device Testing (Infographic)

In 1996, the Health Insurance Portability and Accountability Act (HIPAA) defined standards for safeguarding the sensitive, confidential data of all patients. The act requires health insurance providers to enforce strict privacy and security rules, each designed to protect the patient and all electronically protected health information, known as ePHI.

Organizations should understand how the CI/CD pipeline works before implementing a framework that could help them streamline production processes to reduce bugs and release software products faster. For a successful implementation, technical teams need to be mindful of how DevOps and agile methodologies work together to support an effective CI/CD pipeline.

The future of healthcare is digital. Although, services like telehealth appointments and electronic health records have become the industry norms, providing these services alone are not enough to stay ahead of the competition. It is equally important to invest time and effort to test your medical devices for accurate diagnosis, prevention and treatment of illnesses due to the increasing complexity of software embedded in these devices. Various factors like regulatory norms, cyberattacks or software glitches can affect the functionality of medical devices, and hence, to ensure high-quality output, quality assurance has become the need of the hour.