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Erica Conway
Erica Conway
Research and Development Scientist | GSK
California, Los Angeles, United States
Erica Conway
Summary
Erica Conway is a seasoned professional with over 20 years of experience in Regulatory Affairs, specializing in Pharmaceuticals and In Vitro Diagnostics (IVD). Currently serving as Vice President of IVD Regulatory Affairs for Europe, she has a proven track record in leading teams and managing complex regulatory processes for medical devices. Her expertise encompasses a wide range of topics including CE marking, FDA submissions, and risk management strategies. Erica has successfully expanded consultancy services in the IVD sector, demonstrating a keen ability to navigate regulatory landscapes across Europe and the US. She holds a PhD in Neurophysiology from the University of Bristol and a BSc in Physiology from The University of Sheffield. Erica's leadership experience is complemented by her technical acumen, making her a pivotal figure in her field. She is passionate about driving innovation while ensuring compliance and safety in medical device development. Outside of work, Erica is likely to engage in activities that promote health and wellness, reflecting her professional commitment to improving patient outcomes.
Erica Conway
Work Experience
Director, Global Regulatory Affairs, Precision Medicine & Digital Health at
GSK
November 2024 - Present
Erica Conway
Education
University of Bristol, PhD, Neurophysiology
January 1997 - January 2001
The University of Sheffield, BSc (Hons), class I, Physiology
January 1993 - January 1997
Frequently Asked Questions about Erica Conway
What is Erica Conway email address?
Erica Conway's primary email address is *******@mcra.com. To view the full verified email and additional contact details, sign up for free with Muraena.
What company does Erica Conway work for?
Erica Conway is a Research and Development Scientist at GSK.
Where Erica Conway graduated from?
Erica Conway holds a degree in null from University of Bristol.
How can I directly contact Erica Conway?
To contact Erica Conway directly, you can use the email address *******@mcra.com. Complete contact information is available upon registration with Muraena.
Who is Erica Conway?
Erica Conway is a seasoned professional with over 20 years of experience in Regulatory Affairs, specializing in Pharmaceuticals and In Vitro Diagnostics (IVD). Currently serving as Vice President of IVD Regulatory Affairs for Europe, she has a proven track record in leading teams and managing complex regulatory processes for medical devices. Her expertise encompasses a wide range of topics including CE marking, FDA submissions, and risk management strategies. Erica has successfully expanded consultancy services in the IVD sector, demonstrating a keen ability to navigate regulatory landscapes across Europe and the US. She holds a PhD in Neurophysiology from the University of Bristol and a BSc in Physiology from The University of Sheffield. Erica's leadership experience is complemented by her technical acumen, making her a pivotal figure in her field. She is passionate about driving innovation while ensuring compliance and safety in medical device development. Outside of work, Erica is likely to engage in activities that promote health and wellness, reflecting her professional commitment to improving patient outcomes.
Erica`s contact details
*******@mcra.com
************@bsigroup.com
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