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Regulation, Clinical and Software for Medical Devices

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November 5 - 7, 2024
The Royal Sonesta Minneapolis DowntownMinneapolis, Minnesota

Danyel Carr
Senior Director, Clinical Affairs at Argon Medical
Speaker

Profile

Danyel is a seasoned clinical research expert with two decades of hands-on clinical affairs experience in both the medical device and pharmaceutical sectors. She has served in multifaceted roles across a range of multinational corporations, specializing in areas such as clinical strategy, operations, data management, regulatory compliance, and business development.

Currently, Danyel spearheads the direction and management of Global Clinical Affairs for Argon Medical Devices, a multinational medical device manufacturer and sales organization with a footprint in 114 countries, including a direct organization in China. A critical component in her role is managing a team responsible for the technical documentation required for international product registrations as well as heading all clinical research and trial initiatives. Danyel has an extensive background which also includes leading global clinical studies and providing regulatory guidance for CE marking of medical devices.

Certified as a Clinical Research Associate by the Association of Clinical Research Professionals in 2005, Danyel holds a bachelor’s degree in biology and a master’s degree in clinical research management. She further enriched her academic credentials by completing a post-Baccalaureate program in Medical Science.

A prolific contributor to the field, Danyel has authored multiple articles and is an active member of several professional organizations. She is excited to share her knowledge and insights as a speaker at this year's conference.

Agenda Sessions

  • Reasoning with Requirements: Clinical Data Across the Globe

    8:40am