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  1. Sessions
  2. Ryan Belaney

Ryan Belaney

Ryan Belaney, is the Vice President of Clinical & Regulatory Affairs for Active Implants, LLC. Mr. Belaney is a biomedical engineer, and regulatory, clinical, and quality leader with over 18 years of diverse medical device experience. His expertise includes an established rapport with FDA and CMS via clinical, regulatory, reimbursement, quality assurance interactions and full-cycle product development. Previously, Mr. Belaney was Director of Applied Research with RTI Surgical, Sr. Director of Regulatory Affairs and Quality Assurance at AgNovos Healthcare, and held roles of increasing responsibility at Wright Medical Technology and Osteotech, Inc. Mr. Belaney invests in the MedTech community as a mentor in the Zero-to-510 accelerator and is the Vice President of the Board of Directors for the Orthopaedic Surgical Manufactures Association, OSMA. He earned his Bachelor’s degree in Biology and Chemistry from the University of Mount Union and his Master’s degree in Biomedical Engineering from the University of Toledo.

Today

regulations in orthopedics

OSMA Update: Regulatory Initiatives in the U.S. and EU

What initiatives are shaping the orthopedic device regulatory landscape in the United States and European Union? OSMA representatives will discuss FDA's stance on MR labeling & testing and biocompatibility. They'll also offer insight from Notified Bodies on the EU MDR implementation.

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