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Watch this video recording to learn more about implementing Agile while maintaining compliance in highly regulated medical device development. In such safety-critical industries, product safety, reliability and quality are vital, and therefore compliance with relevant standards is a fundamental requirement. To comply with standards such as IEC 62304, ISO 14971, IEC 60601 and various FDA regulations, developers are required to ensure full process control, traceability, transparency and process visibility, as well as comprehensive documentation of their processes. This webinar recording gives you practical guidance on how to achieve all of the above in an Agile environment.

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