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Chris Sharpe

Chris Sharpe

VP, Regulatory Affairs | Quell Therapeutics

Chartridge, England, United Kingdom

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Chris Sharpe

Summary

Chris Sharpe is a seasoned professional in regulatory affairs with a rich background that spans over 15 years in the pharmaceutical industry. He began his career as a pharmacist before transitioning into regulatory roles, gaining experience as a pharmaceutical assessor at the MHRA and working with major companies like GSK, Wyeth, and Allergan. His leadership skills were honed at Biogen, where he built the regulatory department for the UK and Irish affiliate and later served as a Global Regulatory Lead. Currently, as the VP of Regulatory Affairs at Quell Therapeutics, Chris drives innovative regulatory strategies in the biotechnology sector. His expertise encompasses clinical development, drug formulation, and regulatory submissions, making him a crucial player in advancing therapeutic solutions. Chris's journey reflects a commitment to excellence and a deep understanding of regulatory landscapes, which is essential for navigating the complexities of drug development and compliance.

General

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Technical Background

Leadership Experience

Long-Term Tenure

Professional interests

Industry-specific interests

Emerging Technologies

Leadership Development

Organisational experience

Corporate Experience

Consulting Experience

Chris Sharpe

Work Experience

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VP, Regulatory Affairs at

Quell Therapeutics

December 2021 - Present

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Head Of Regulatory Affairs at

Quell Therapeutics

September 2019 - December 2021

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Global Regulatory Lead at

Biogen

July 2018 - September 2019

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Associate Director, Regulatory Affairs, UK and Ireland at

Biogen

July 2015 - July 2018

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Director, Regulatory Affairs (EU) at

Kuur Therapeutics

December 2012 - July 2015

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EU Regulatory Affairs Senior Manager at

Allergan

January 2012 - December 2012

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Regulatory Affairs Manager at

Allergan

November 2010 - December 2011

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Pharmaceutical Assessor at

Medicines and Healthcare products Regulatory Agency

February 2009 - November 2010

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Regulatory Affairs Officer at

Pfizer

June 2008 - January 2009

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Regulatory Executive at

GSK

September 2006 - June 2008

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Locum Pharmacist at

LloydsPharmacy

August 2005 - September 2006

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Chris Sharpe

Education

University of Nottingham, Master's Degree

January 2000 - January 2004

University of Nottingham, Master's Degree

Frequently Asked Questions about Chris Sharpe

What is Chris Sharpe email address?

Chris Sharpe's primary email address is ********@quell-tx.com. To view the full verified email and additional contact details, sign up for free with Muraena.

What company does Chris Sharpe work for?

Chris Sharpe is a VP, Regulatory Affairs at Quell Therapeutics, a company specializing in Commercial physical research.

Where Chris Sharpe graduated from?

Chris Sharpe holds a degree in Pharmacy from University of Nottingham.

How can I directly contact Chris Sharpe?

To contact Chris Sharpe directly, you can use the email address ********@quell-tx.com. Complete contact information is available upon registration with Muraena.

Who is Chris Sharpe?

Chris Sharpe is a seasoned professional in regulatory affairs with a rich background that spans over 15 years in the pharmaceutical industry. He began his career as a pharmacist before transitioning into regulatory roles, gaining experience as a pharmaceutical assessor at the MHRA and working with major companies like GSK, Wyeth, and Allergan. His leadership skills were honed at Biogen, where he built the regulatory department for the UK and Irish affiliate and later served as a Global Regulatory Lead. Currently, as the VP of Regulatory Affairs at Quell Therapeutics, Chris drives innovative regulatory strategies in the biotechnology sector. His expertise encompasses clinical development, drug formulation, and regulatory submissions, making him a crucial player in advancing therapeutic solutions. Chris's journey reflects a commitment to excellence and a deep understanding of regulatory landscapes, which is essential for navigating the complexities of drug development and compliance.

Chris`s contact details

mail

********@quell-tx.com

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