Founder and Chief Executive Officer of the World Medical Device Organization
Modules
Medical Device Regulatory Affairs and Quality Assurance
Module 7 - Clinical Evaluation for Medical Devices
Biography
With over 30 years of experience, Ms. Danielle Giroud is an internationally recognized clinical research and regulatory expert within the global medical device industry. She has shared her extensive knowledge and experience with multi-national companies, organizations, and start-ups from around the world to help bring their products to market quickly and efficiently.
Ms. Giroud is also known for her contribution and engagement as founder and senior faculty board member of the World Medical Device Organization (WMDO), as well as a convener for the expert group on clinical investigations (TC 194 WG4) for the ISO 14155, and liaison with the EU Commission - Clinical Investigation and Evaluation (CIE) task force and other regulatory authorities throughout the world.
