Join us for an exclusive Executive Briefing designed for medical device companies, featuring Sonatype and ASERVO Software. This event will focus on leveraging software solutions to help medical device manufacturers comply with evolving regulations such as the Medical Device Regulation (MDR) and the European Database on Medical Devices (EUDAMED).

Key Topics

Simplify MDR Compliance with Automation: Learn how the Sonatype solution can automate compliance workflows, from managing clinical data to conducting real-time audits. Discover how automating risk management and reporting can streamline the path to MDR certification and improve regulatory efficiency.

Reduce Compliance Costs and Complexity: ASERVO Software, in partnership with Sonatype, will demonstrate how to reduce the cost and complexity of maintaining compliance by deploying a secure software supply chain, ensuring that all components of your medical devices are tracked and meet regulatory standards from development to post-market surveillance.

Traceability and Post-Market Surveillance: Understand how Sonatype’s automated solutions can enhance post-market monitoring and reporting, allowing for faster identification of risks and compliance with MDR’s vigilance requirements. ASERVO will guide you on implementing systems that facilitate smooth reporting to EUDAMED.