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Erica Conway

Erica Conway

Research and Development Scientist | GSK

California, Los Angeles, United States

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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.

General

Specialist

Technical Background

Leadership Experience

Long-Term Tenure

Professional interests

Leadership Development

Emerging Technologies

Innovation

Organisational experience

Corporate Experience

Consulting Experience

Erica Conway

Work Experience

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Director, Global Regulatory Affairs, Precision Medicine & Digital Health at

GSK

November 2024 - Present

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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

mail

*******@mcra.com

************@bsigroup.com

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