Glenda Marsh

Glenda Marsh

Panelist

Senior Director of Policy Implementation Global Regulatory Affairs Policy and Intelligence,

Johnson & Johnson Medical Devices

Ms. Marsh is an accomplished, proactive and versatile corporate professional with over 18 years of global experience in regulatory affairs, program management and operations across the healthcare industry. She has successfully established and led teams to support the implementation of regulatory changes with significant business impact. Since 2016, she has led the J&J Medical Device Regulatory Affairs efforts in preparing for and executing to the new EU MDR requirements. Since joining Johnson & Johnson in 2001, she has held positions of local, regional and global responsibility and covered different J&J sectors, companies, functions and regions (Latin America, North America and EMEA). Ms. Marsh has led regulatory programs from concept to approval and implementation, spanning the entire medical device product lifecycle. She has a Master’s degree in Chemical Engineering from Stevens Institute of Technology and a Bachelor’s Degree in Chemical Engineering from the Polytechnic School of the University of Sao Paulo.

My Session

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June 15,2021

EU MDR: Tackling Today’s Challenges

1:00 pm-2:30 pm

Room 45