2024 - Medical Device Safety: The Next Frontier
Date2024-10-23
Deadline2024-10-23
VenueONLINE-VIRTUAL, USA - United States
KeywordsMedical Device; Medical Device Safety and Regulation; Medical Device Design
Topics/Call fo Papers
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.
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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.
Keywords: Medical Device, Medical Devices, Diagnostics, Medical Device Regulation, Medical Device Manufacturing, Laboratory Technology, Medical Device Safety, Medical Device Development
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.
Read more...
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.
Keywords: Medical Device, Medical Devices, Diagnostics, Medical Device Regulation, Medical Device Manufacturing, Laboratory Technology, Medical Device Safety, Medical Device Development
Other CFPs
- Operationalizing Innovative Biomarkers to Support Evolving Therapeutic and Diagnostic Landscape for Neurodegenerative Diseases
- Safety-focused from Start to Submission: A Story of Target Safety Assessment and ICH S1B (R1) Guidelines
- Considerations on the Evolving Testing Requirements for Environmental Fate Studies
- Embracing a Culture of Quality: Establishing and Maintaining Effective CRO Oversight
- Revolutionizing Biomarker Development: Automated Detection and Isolation of Extracellular Vesicles
Last modified: 2024-09-17 05:18:00