are you designing complex medical devices with safety-critical embedded software? do you need to comply with fda, mdr, or ivdr regulations and standards such as iec 62304? if the answer is yes, you can use matlab® and simulink® for:
- requirements management and traceability
- automating verification and validation
- rapid prototyping and system-level testing
- comprising the technical documentation file
free workflow assessment
mathworks experts will evaluate your existing medical device development workflow and give guidance to improve the integrity and quality management of the process. the assessment gives you an expert opinion and suggested next steps for improving your workflow. this will help your organization to:
- manage risks and avoid common mistakes
- reduce development time and costs
- shorten time-to-market for new products
why mathworks?
mathworks is a trusted engineering partner and solution provider for the largest medical device and pharmaceutical companies in the world. our advisory and engineering services are delivered by senior-level technical experts with knowledge gained from years of collaboration with leading companies in the industry.