In this free webinar, learn how to improve medical device safety by streamlining the development and regulatory process for medical devices. Attendees will learn about the information required to be able to identify non-clinical safety and performance requirements. The featured speakers will share how to use standards that are applicable to products. The speakers will also discuss the role of accredited testing facilities and how to access them.
TORONTO, Oct. 7, 2024 /PRNewswire-PRWeb/ -- During the COVID-19 pandemic, there was global demand for engineered medical devices and a shortage of critical products, including ventilators. Many countries, including the UK, resorted to developing new products or scaling up existing ones to meet their needs.
Given the critical urgency for products, regulatory processes and expectations had to be adapted. The expert speakers were involved in the UK Ventilator Challenge and one key challenge was understanding the non-clinical safety and performance requirements.
They observed first-hand the collaborative efforts of extraordinary individuals who had a broad range of backgrounds: Clinicians, Design Engineers, Test Engineers, Quality Engineers, Regulatory Affairs Specialists, Scientists and academics.
Element RegNav is a software solution designed to navigate these complex requirements, enabling the development and maintenance of safe and high-performing medical devices. This approach leverages the foundation of international safety and performance requirements and establishes state-of-the-art practices and user-defined characteristics derived from the intended use and technological features of medical products.
From defining product characteristics to understanding the performance, safety, usability and functional requirements, RegNav helps create comprehensive design and development plans. These plans ultimately facilitate submissions to regulatory authorities, notified bodies and stakeholders, providing evidence that all necessary requirements have been met.
This project represents not just a technological advancement but a profound commitment to improving the safety and efficacy of medical devices, ensuring better outcomes for patients and healthcare providers worldwide.
Register for this webinar today to discover how Element RegNav can improve medical device safety by streamlining the development and regulatory process for medical devices.
Join experts from , James Pink, Director, Medical Technologies; and Michael Kipping, Director, Medical Technologies, for the on Wednesday, October 23, 2024, at 1pm EDT (10am PDT).
For more information, or to register for this event, visit .
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