With increasing market pressure to develop complex, high-quality medical products as quickly as possible, compliance with medical device regulations and standards is becoming increasingly challenging. Medical device developers around the world are faced with the problem of maintaining and improving product safety, reliability and compliance with standards such as IEC 62304 (life cycle processes) and ISO 14971 (risk management), among others, while shortening development times. Implementing mature processes to achieve continuous and automated compliance helps reduce time to market and represents a significant competitive advantage for medical device companies.

Watch our webinar recording to learn how to manage compliance in the rapid development of medical devices, including topics such as:

– Maintaining quality while reducing development time for medical technology
– Mature process control and traceability
– Risk management according to ISO 14971 and compliance with IEC 62304

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