In today’s digital age, software validation is critical to ensure the reliability and safety of medical devices and IVDs in accordance with industry standards such as IEC62304, TIR 57, IEC 80002-3, ISO TIR80002-2.
Our validation services cover all aspects of the software used in medical devices, from design to implementation. We follow strict protocols to ensure that your software meets all regulatory standards, reducing risk and improving patient safety.
Are you ready to take the next step to ensure that your medical devices and IVD products comply with EU and FDA regulations?
Contact us today to schedule a consultation and find out how we can help you achieve your goals.